Tag | Content |
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EnhancerAtlas ID | HS082-00142 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:9359600-9364390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr1:9363780-9363791 | TATGACCTTGA | - | 6.62 | Esrrg | MA0643.1 | chr1:9363781-9363791 | ATGACCTTGA | - | 6.02 | FOSL2 | MA0478.1 | chr1:9360370-9360381 | CTGAGTCACCC | - | 6.02 | HNF4G | MA0484.1 | chr1:9362643-9362658 | TGGCCTTTGGACTCT | - | 7.58 | JUNB | MA0490.1 | chr1:9360370-9360381 | CTGAGTCACCC | - | 6.02 | Myog | MA0500.1 | chr1:9361025-9361036 | GACAGCTGCAG | + | 6.62 | NFE2L1 | MA0089.2 | chr1:9360366-9360381 | TTTGCTGAGTCACCC | - | 6.88 | Nfe2l2 | MA0150.2 | chr1:9360368-9360383 | TGCTGAGTCACCCTA | - | 6.76 | RORA | MA0071.1 | chr1:9363782-9363792 | TGACCTTGAT | - | 6.02 | Tcf12 | MA0521.1 | chr1:9361025-9361036 | GACAGCTGCAG | + | 6.14 | USF1 | MA0093.2 | chr1:9363465-9363476 | ACCACGTGACC | + | 6.32 | USF2 | MA0526.2 | chr1:9363463-9363479 | CAACCACGTGACCAGT | - | 6.1 | ZNF263 | MA0528.1 | chr1:9361064-9361085 | GAAGGATGGGGGTGAAGGGAA | + | 6.44 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_00563 | chr1:9361755-9364768 | Adipose_Nuclei | SE_01570 | chr1:9359845-9363523 | Aorta | SE_01570 | chr1:9363656-9366696 | Aorta | SE_23490 | chr1:9359796-9361335 | Colon_Crypt_1 | SE_23490 | chr1:9362746-9363598 | Colon_Crypt_1 | SE_23818 | chr1:9359897-9361251 | Colon_Crypt_2 | SE_24876 | chr1:9359985-9361543 | Colon_Crypt_3 | SE_26458 | chr1:9359877-9361291 | Duodenum_Smooth_Muscle | SE_26458 | chr1:9361668-9364426 | Duodenum_Smooth_Muscle | SE_26667 | chr1:9359663-9361407 | Esophagus | SE_26667 | chr1:9361744-9363493 | Esophagus | SE_32227 | chr1:9359984-9361097 | Gastric | SE_32227 | chr1:9362378-9363428 | Gastric | SE_45049 | chr1:9359811-9361082 | NHLF | SE_45049 | chr1:9362570-9363503 | NHLF | SE_50208 | chr1:9359830-9361115 | Sigmoid_Colon | SE_50208 | chr1:9361719-9363620 | Sigmoid_Colon | SE_52461 | chr1:9359718-9361526 | Small_Intestine | SE_52461 | chr1:9361723-9363621 | Small_Intestine | SE_52461 | chr1:9363622-9364757 | Small_Intestine | SE_65576 | chr1:9362424-9363473 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009298 | chr1 | 9358616 | 9364232 |
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Enhancer Sequence | CAATCTCGGC TCACTGCAAC CTCCGCCTCC CGGGTTCAAG CAATTCTCCT GCTTCAGCCT 60 CCTGAGTAGC TGGGATTACA GGCATGCGCC ACCACACCCA GCTAATTTTT TGTATTTAGT 120 AGAGACAGGG TTTCACTATG TTGGTCAGGC TGGTCTTGAA CTCCTGACAC CAAGTGATTC 180 ACCCGCCTTG GCCTCCCAAA GTTCTGGGAT TACAGGCATG AGCCACTGCG CCCGGGCCGA 240 CATCATCTCT ATAAATTTTT TTTTTTTTTA AATTAGCCAG GCATGATGGT GTGTGCCTGT 300 GGTCCCAGCT ACTTGGGTGG CTGAGGTGGG AGGATCGCTT GAGCCTAGGA GGTCAAGACT 360 TGCAGTGAGC AGTGATTGTG TTACTTTACT CCAACCTGGG CAACAGAGTA AGACCCTGTC 420 TCAAAAAAAA AAAAAAAAAA AGGGTCTCAT GCTGGTCCAT TACATTGATG TCATCATGCT 480 TCATTGGACC TAGTGAGCAA GAAGTCGCAA CCACTGTAGC CTTATTGGTA GGACATTTAC 540 ATGTCAAGCG ATGGGAAATA AATTCTACTG AAATTCGGGG ACCTTCTCCC TTAGTGAAAT 600 TTCTCGGGGT CCAGTAGTGT CAGGCCTGTG AAGGTATCCC CTCTAAGGTG AAGAATAAGT 660 TGTTACAGCT TTCCTCCTGC AACCAAGAAA GAGGCACAAT GCCTCGTGGG CCTGTTTGGA 720 CTTTGGAGGC AACACATTCC TCATTTGGGT GTGTTACTCC AGCCCATTTG CTGAGTCACC 780 CTAACGCTTC TAGTTTTGAG TGGGGCCCGT AGCAGAAGAC TGCAACAGGT CCAGGTTGCT 840 GTGCAACCTG CTTTGCCACT TGGGCCACCA GCAGATCCAG TGGTGGTTGA GGTCAGCGGC 900 AGACAGGGAG GCTGCTTAAA GCCTTTGGCA GGCCCCTGTA GATGAATCGC AGTACAGGCC 960 TTGGGATTTT GGAGCAAGGC CCTGCCATCA TCCACAAATA ACTTCATTCC TTTTGAGAGA 1020 CAGCTCTTGG CCTAATACTG GACCCTAGTA GAGACTTAAT GTTTGACCAT CAGCCACGAA 1080 GTTGCCATGT GACCTGAGCT GCCCATCATG AAGTGGGTGT TATCTATGAT CTGACCGACC 1140 AAACCAGACA TTGGGCATGT GTGGCAGAAC GCTGCCATCG AGAGGAAGTG GTATATATGG 1200 GATCAGGTCT GAGCAGGTCC TGAAGGCACA AGTAAGTGAC ATGAGGAAGT GGTCCAAAGG 1260 CCCATGGTTC TTACTTTGCC CACTGCCTTC TCTCTCCAGC CTGTATCTAT GGTCTCCTGG 1320 GGAGTTCCCT CTGATCGATT GACAGTGGAA GAGAAGACTT AGTCAGCCTG GTTTGCAGAT 1380 GGCTACAGAT GGCTCTGCAC TATATGAAGG CACAACCCGA AAGTGGACAG CTGCAGCACT 1440 ATAGCCCCTT GCTGGGACAC CTCTGAAGGA TGGGGGTGAA GGGAAATCCT CCCTGGCAGA 1500 GCTTCGGGCA GTGCACCTGG TTGTGCACCT TGCTTCGAAG GAGAGATGGC CAGATGAGTG 1560 ATTATATACT GATCCATGGG CTGTGCCTGA TGATTTGGCT GGATGGTCAG GGATTTGGGG 1620 ACTTGGAAAG AGTATGATTG GAAGATTGGT GACAAAGAAA GCTGGGGGCC TGGCATAGTG 1680 GCTCACACCT GTAATCCCAG CACTTTGGGA GGCCAAGGTG GGAGGATTGC TTGAGCCCAA 1740 GGAGTTCGAG ACCAGCCTGA GCAACATAGT GAGACTCCCC GCCCCCGCCA TCTCTACAAA 1800 AATAAAAAAT TAGCTGGGCG TGGTAGCTCA TGCCTGCAGT CCCAGCTACT TGGGAGGCTG 1860 AGGTGGGAGG ATCACTTGAG CCTAGGAGGT TGAGGCTGCA GTGAGCTGTG ATTGCTCCAG 1920 CCTGGGCAAC AGAATGAGAC CCTGTATCAA AAAACCCAAC CAAACAAAAA AGCAATTGGG 1980 GGAAGATGTA TGTGGATAGA CCTGAGTGCG CACAGGACAC GGATAGACCT CCCGAGTGCG 2040 CACAGGACAT GAGGTATGTG GGTAGGATGA CCTAGGTGGA TTCTCGTCAG CCTCTTTCCC 2100 TGGCCACCCC TGTCATCGCC TGGTGGGCTC AGGAACAAAG TGGTCATGGT GGCAGAGATG 2160 GAGGTGATGC ATGGGCTCAG CAGCATGGAC TGCCACTCAC CAAAGCCGAC CTGGCTATGG 2220 CTACCACTGG CTGCTAGTCT GCCAGAAGCG GAGACTAACA CTGAGCTCCA GTATGGCCCC 2280 ATTCCCCGGG ATGATCACTG CACCTGGTGG AAGGCACATT GGACCACTTC TGTTTTGGAA 2340 GGGGCAGCGT TTTGTCCTTA CTGGAGCAGG CACTTATTCT GGATACAGAT TCGTCTTCCC 2400 TGCACACAGT GCTTCTGCCA AAGTCACCAT CCATTGATTG ACAGAACACC TTTCCCACTG 2460 TCACGCTGTC CGTGTAGCAC TGCTTCCAGG GAGCTCACTT CACAACCAAG GAAGTGTGGC 2520 ACTGGGATCA TGTGCAGGGA ATTGGCCGGT GAGCACGAGC CCACTGGTTT CGCCTATCAT 2580 GCTAAGTGGA ACTACGGTCT TGTTATTGCC TTTATTTGGA AATTAAGTAT GGTTTAAGAA 2640 GATGCCAGTG GGTGCCTATG GGTGCCAGTT GGTAAGGGGT GGACCTGTGA TGATTGATTT 2700 TGGATGTCAA CTTGACTAGA TTAAGGAATA CCCAGGTAGA TGGTAAAGCA TTGATTATTC 2760 TCTATGCTTC AGTACACACT GAGCCTGTCC CTTTTCTGCT GACAGGGAAG CCCAGTGGTT 2820 TGACATTGTG TAGAATGATC GGGCTGCCCC AGATGTGTCT GTGAGGGTGT TTTTGGAGGA 2880 CACTGGCAAT TGAGTCACTC AACTGGGTGG GGAGGATCTG CCCTCCATGT GGGCAGGCAC 2940 CATCCAGTCA GCCGGGGGCC TGGAAGAAGG GTGAATCCTG GCTCTCTGTC CCGGAGCTGG 3000 GATGCTCTTC TCCTGCGCTT GGATGTCAGA ACTCCAGGTT CTCTGGCCTT TGGACTCTGG 3060 GACTCGTACG AGTGGTCTCC GGAGTCTTTG ACCTGGGACT GGGAATGACC ACGTTCCCCA 3120 CCATCCTGAA GCAGCTGACT TGAAAGAAGG GCAGTAGAGT CTTTTGAAGT TGCAATTACA 3180 ATGCCAGCTA GGTGACAATA CTTTGTAGGG CTGGGTCAGG GGTCTTCAAA AGGCTCTATG 3240 TACTCTGTAT CAGCATCCAA TATATGGTGC TGGTTTCTCC CGTAGCCAGG ATTCACGGGT 3300 CCAGGAATCA AGGGGAGGAA ATGGGAGTGG CACTGCGCAT CATATCCCCT AGGGACCCGC 3360 TAGCGAAATT GTTGCTTCCT GTTCCTGTGA CTTTATGCTC TGCTGGCCTG GAGGTCTTGG 3420 TTCCAGAGAG AGGAATGCTC CTACCAGGAG ACACAACAGT GATTCCATTG AACGGGGGGT 3480 AAGGCTGCCA CCTGGCTTCT TTGGGCTCCC TGTGCCTCTG GGTCAGCAGG CTGAGAGGGG 3540 AGTGATGGTG TTGGCTGTGG AGATTGATCT GGACTACCAA GGGGAAATTG ATCTGGACTG 3600 CTCCACAATG AGGCAAGGAA GAGTGTGTCT GGAGTACAGG ATACTCCTTA GGGCATCTGT 3660 TAGTATTACC ATGCCCTGTG ATTAAGTCAA TGGGAAATTA CAAGGATACA ATCCAGGCAG 3720 GACTGTGAAT GACTCAGACC CTTCAGGAAT GAATGTTTGG GTCACTCTGC CACTTAAAGA 3780 ACCACAGCCA GCTGAGGTGC TTGTTGCAGA CGAAAGGAAC ACAGAACAGG ACAGAGGGAG 3840 GTAGTTATAA TAAATACCAG CTCCAACCAC GTGACCAGTT ACAGAAACAA GGGCCAGAAT 3900 TGCTGGGAGT ATTTCCTCCC TATTTTGTTC AGAATACGGT TGTATGCATT TACATGTATA 3960 TTAGGCAAAT ATCTGTTTTC TTTCCTCTCT TACTCCTTAT TCTTAGAACA TGTGTTGAGT 4020 CTATAGCAGT ATTTAAGTAT TAATTTTACA TCATAGTATT TAAGTTATTG AGTATCAGAG 4080 GAGAGAGGAG TGAATAGCAC TCAAGGACTG TACCTCCTCT CTGGAGAAGG GATTAATGTG 4140 TCTTTGCTAT GCAGGATAGT AGTGTCACGA TAGGTGGAAC TATGACCTTG ATACTGTCCT 4200 TGGAGATTAA GTATGGTTTA AGGAGATGCC AGTGGGTGCC TCTGGGTGCC AGTTGATAAG 4260 GGGCGAACCT GTGATGATTG ATTTCAGATG TCAACTTGAC TAGACTAAGG AATACCTGGA 4320 TAGATGGTAA AGCATTGATG ATTCTCAATG CTTCAGCACA CACTGAGCCC ATCCCTTTTC 4380 TGCTGACAGG GAAGCCCAGT GGTTTGGCAT TTGTGTAGAA TGATTGGGCT GCCCCAGGTG 4440 TGTCTGTGAG GGTGTTTTTG GCATTGGAGT CACTGGACTG GGCAGGGAGG ATCTGCCCTC 4500 CATGGGGTCA GCCACCGTCC AATCAGCTGG TGGCCTGGAT GGAACAAAAA GCTGGAAGAA 4560 GGGCGAATCC TGGCTCTCTG TCCCGGAGCT GGGACATCCT CCTTCTCCTG CACTCGGATG 4620 TCACAACTCC AGGTTCTCTG GCATTTAGAC TCTGGGACTC ATACCATTGG TCCCCGGGGT 4680 CTTTGGCCCG GGGCTGAGAA TGACCCCATT GGTCTCCCTG GTTCTGAGGC CTTCAGACTT 4740 GGCTGAGCCA CACTCCTGGC TCCCCTGGGT CTCCAGCTTG CAGATGGCCT 4790
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