Tag | Content |
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EnhancerAtlas ID | HS102-00258 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:16506030-16510350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr1:16510043-16510053 | GGTCACGTGC | + | 6.02 | ELF3 | MA0640.1 | chr1:16508229-16508242 | CTACTTCCGGCTA | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr1:16508479-16508497 | GGGAGGAAGGAAGCAGAG | + | 6.42 | LMX1B | MA0703.2 | chr1:16507192-16507203 | ATTTTAATTAA | + | 6.62 | Lhx3 | MA0135.1 | chr1:16507206-16507219 | AAATTAATTATTT | + | 6.78 | Nr2f6(var.2) | MA0728.1 | chr1:16509417-16509432 | GAGGTCAGGAGTTCA | + | 6.22 | PBX1 | MA0070.1 | chr1:16506438-16506450 | ATTGATTGATGG | - | 6.62 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16507977-16509332 | Colon_Crypt_1 | SE_24743 | chr1:16508183-16508861 | Colon_Crypt_3 | SE_26540 | chr1:16504790-16512175 | Esophagus | SE_28102 | chr1:16507825-16509373 | Fetal_Intestine | SE_29455 | chr1:16507734-16509371 | Fetal_Intestine_Large | SE_31527 | chr1:16507486-16509710 | Gastric | SE_31527 | chr1:16509851-16511737 | Gastric | SE_34268 | chr1:16506936-16512113 | HCT-116 | SE_34628 | chr1:16506549-16512234 | HeLa | SE_36144 | chr1:16507720-16509431 | HMEC | SE_38062 | chr1:16507125-16509874 | HUVEC | SE_40833 | chr1:16507342-16509479 | Left_Ventricle | SE_44998 | chr1:16507356-16509449 | NHLF | SE_46140 | chr1:16507347-16510631 | Osteoblasts | SE_47009 | chr1:16508039-16509386 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16507961-16508560 | Pancreas | SE_47539 | chr1:16508587-16509159 | Pancreas | SE_48744 | chr1:16507441-16509527 | Right_Atrium | SE_50427 | chr1:16507395-16509522 | Sigmoid_Colon | SE_52536 | chr1:16507445-16509419 | Small_Intestine | SE_56795 | chr1:16506234-16507286 | VACO_400 | SE_56795 | chr1:16507333-16512008 | VACO_400 | SE_57357 | chr1:16508000-16508578 | VACO_503 | SE_57357 | chr1:16508592-16509318 | VACO_503 | SE_57939 | chr1:16507977-16509011 | VACO_9m | SE_64726 | chr1:16507942-16511421 | NHEK | SE_65472 | chr1:16507356-16509554 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 16508086 | 16509162 | chr1 | 16509950 | 16510149 | chr1 | 16508402 | 16508642 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | TGTAAATGAA GAACCTGAAG CCCAGAAGCC CAGAGAGTGG AAGTGATTTG ACCAAGGTTT 60 TTTTTTTATT ATTATTATTA TTATTATTTT ATTTTTTTAG ACAGAGTCTC ACTCTTGTCG 120 CCCAGGCTGG GGTGCAGTGG TGCAATCTTG GCTCACTGCA ACCTCCACCT TCTGAGTTCA 180 AGTGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCGCCCA CCACCACGCC 240 TGGCTAATTT TTGTACTTTT TTTTAATAGA GACAAGGTTT CAACATGTTG GCCTGGCTGG 300 TCTCAAACTC GTGACTTCAG GTGATCCGCC CTCCTCGGCC TCCCAAAGTG CTGTGATTAC 360 AGGCGTAAGC CCCGCGCCCA GCCAAGGTTA TTCATTTGTT CAGAAAACAT TGATTGATGG 420 GGAACTTTTG TTGAGTAGAG TTTCAGTTTG GGATGATGAA AAAGTTCTGC AGATGGACGG 480 TGGCGAAAAG TTGCACAGCA ATGTGAATGC ACTTAATGCC ACCGACCTGT ACACTTCCAA 540 ACGCTTAACA TGGTCGATTT TATGTTACAT ATATGTTACC ACCATAAAAA CACAAATGAA 600 AAAGATTTAC TGGGCCGGAC ATGGTGGCTC ACACCTATAA TCCCAGCACT TTGGGAGGCT 660 GAGGCAGGCA GATCACTTGA GGTCAGGAGT TCGAGACCAG CCTGGCCAAC ATGGTGAAAC 720 CCCGTCTCTA CTAAAAATAC AAAAATTAGT CAGGCGTGGT GCTGCACACC GTGGTGCAGC 780 TACTCGGGAG GGTAAGGCAG GAGAATCACT TGAGCCCGGG AGGTGGAGGT TGCAGTGAGC 840 CGAGATTGTG CCATTGCACT CTAGACTGGG TGGGTGACAG AGTGAGACTC CATCTCAAAA 900 AAAAAAAAAA AAAAGATTTA CTGGTCCCCT GTTGTGTTTT AGGCATGAGT CAGATGCTGT 960 GGATATAGCA ATGAACACAG CAGACAAAGG TCTCTGCCTC TGTGAAACTG ACATTGGAGA 1020 ACAGCAGTCT AGAAGAACTT GCTGTGGATG GAATGATGAA TGGATAGAAA CGTTTTACAT 1080 CTGCTCCGCA CTGGCCGCAC GCGGCTACTG AGCACTTGAG ATGCGTCTGG TGCACCTGAA 1140 GAGCTGACTT TAATTTTATT TCATTTTAAT TAATTTAAAT TAATTATTTG TTTATTTGAG 1200 ACAGAGTCTC GCTCTGTCAC TCAGGCTGGA GTACGGTGGC GCAATCACAG CTCACTGCAA 1260 CCTCTGCCTT CTGGGCTCAA GCCAGCCTCC TACCTCAGCC TCCTGAGTAG CCAGGACTAC 1320 AGGTGTACAC CACCACACCC AGCTAATTTT TTGCGTGCTT TTTGTAGAGA TGGGGTTTCA 1380 CCATGTTGCC TAGTCTGGTC TCGAACTCCT GACCTCAAGA GATCCACCCA CCTTGGATCC 1440 CAAAATGCTG GGATTACAGG CATGAGCTAC TGCGCCCGGC CTCTAGATTT AAATAGTACC 1500 TACCGAACTG GCCAGTGCAG CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA GAGCTGGGCC 1560 TGGCTGTGTG TTATTCACGT TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC CTCTGGCAGC 1620 AGAATCACCT GGGAAGCCAA AACTTCAGAT CCCTGGGATC CCAGACCCAC TGAATCAGAA 1680 TCTCCGAGGC CAGGGCTTGG GCGTCTGCCC GTTCACCACA CACCCCAGCT GATTCTGATG 1740 CACATGAGGT CAAGTTTGAA ACCCACCCCA CTGCCCTAGT TGTTCAAGAC TCCCAGCGCT 1800 GGCTGGATGC AAAGTCTTAT GCCTGTAATC CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG 1860 ATCACTTGAG GTCAGGAGTT CGAGACCAGC CGGGCCTACA GAGTGAAACC CCGTCTCTAC 1920 TAAAAATACA AAAATTAGCT AGGTGTGGTG GTGGGCGCCT GTAATCCCAG GAGGTGGAGG 1980 TTGCAGTGAG CCGAGATCGC GCCGCTGCAC TGCATCCTGG GCAACAGAGC GGGACTCCGT 2040 CTCAAAAAAA AAAAAAGACT CCCGGCCAGG AAGAGAGCTT GAATGAAGTC TGACCTGCAC 2100 CAGGCCTTCT GGGCCCAGAC CAGGCCTGCT TAGGGGCATG TGCCCTGCTC AGAACTTCCC 2160 CATCCCAGCT AACCCAGAAG ATAGCTGGGA TGAAGATAGC TACTTCCGGC TACCAGCCCA 2220 TGATTCTTTG CCAGCCTGCA CTGTTCCCTG AAGAGCAAAA AGACTTGGAA TTTCCCTGCT 2280 CTATCCAGAG GGGCTGGGAT GAGGGGTCCT GAGTTCCCTT ATCCCATGTC CTACCAACCT 2340 CTGGAGCTCT CCAGTCAGCC AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC AATGGGAGGG 2400 AGAGGCTTGG CCCAGCACCC CACCCCACAG ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA 2460 AGCAGAGGCA GCCTGGGCCA GCGGACACAG GGTTGGGGGT GACACAGGCC TCAGGAATTT 2520 GAAAACAAAC ACTTCGCCAG GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG 2580 CCCAGGTCCC TCCCTTTCAG GGCAGGGGTG AATCCCAGTG CTGCTGACCA TGGCCCCCGG 2640 CTGGACCCAG TGCTCGGGGA GTTTCCACTC CGCTGGTGGG ATGGGAAGGT CATGGGAGGT 2700 GTGGGGGGAT CCAGGCTCTG TCCAGATACG GGAGCATCCT GGCTGGGGTG AGGACAGGAA 2760 GGGACAAAGA GCTGGGAAAG CCACGAGACC CCAGGAGAAG GCTCAGCAGC AACAGGATGC 2820 CGCCTCAAGC ATTTATTGAG CACCCATGGT ATTCCAAAAA CTGAGAATAT AAGCACTGCC 2880 TAGCTGGGGA GATCAGGGGA AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA GGTGGCATTG 2940 AACTGAGCCC TGAAAGGTAA ACTAGGACCG GGGAGGACAG AATCTTACAA GTCTCCCCCC 3000 TTCACACTCC CAGAGCCGGC GCTCAGTGAG TGCATGAGTG AGTAAGCGGC TGACCAGCGA 3060 CTATGCAGCA TGAATGAATG ACAGACTGAA TGACATGAAG CCTGGAGTCT CAAGGCCGAG 3120 ACTGCAAAAG AAGAGTCCAT CCTCCTATCC CCTCTGCTCT GAACTCTCTT CATGATCCTG 3180 AAGGTGCTTG GTACCTGGAG ACTACGGAGC CAGCCTGCCG GGGTTCTAGT CTGAACTCAG 3240 TCACTTCCCA GCTGTGTAAC TTTGGACAAG TTACTTAACC TCTCTGTGCC TCTGGTCCCT 3300 TCTCTGTAAA GTGTAGTCAT CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT 3360 TGGGAGGCCA AGGCAGACGA ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGCCCAACA 3420 TGGTGAAACC CTGTCTCTAC TAAAAACACA AAAATCAGCC GGGTGTCGGG GGCAGGCACC 3480 TGTAATCCCA GCTACTCGGG AGGCTAAGGC ACGAGAATTG CTTGAACCCG GGAGGCGGAG 3540 GTTGCAGTGA GCTGACATCT CGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCAA 3600 AAAAAAAAAA AAAAAATACA GAGGTAATCA TAGTGCCTCC TTCACAGGGT TTTTGAGAGG 3660 ACTGAATGAG TTTTACAAGT GAAGTGCTTA GAACGACGTT GCACATGTAG TGAGAACTAC 3720 ATGAGTGTTG GCCAATGCTA TTACTGAGGT TCCAGCTTAC GCGTTCATTG AGTCACTCAC 3780 TCACTCACTG TTCATTCACT GATTCGCTCC TACATGCCAT CCGCCACTTA CACACCCCTC 3840 CCTCTTCACC GTCATCTGTT AAGCAATCCC CGTGTGCCCG GCTCTCTCCT CTCGGTCCTC 3900 CCAGCCCCCC TTTGCCAGTC TTGGATGGTG CCCGCCGTGC TGCCAATTAC CCTAACAATT 3960 TCATTAATTC CTCTCAAGCC CAAAACAAAC AAGAAGGACC TATCTGGAGC AGGGGTCACG 4020 TGCTAAGACC AGAAGCAGGT GTGGGACAAA CCCTCTAGGA CGAGTTCTTT GACCAGAGTT 4080 CATCACCGGA GCTGCTCCAG AGATGGCCAG GCCTCCCCAC CTGCAGGTGC CCGGCCAGTG 4140 CCCCCCACCC CGGGCAGCCT CACCCACTCC CCTCTTTGAG TAAAGGTAAA GGGACTTGCC 4200 CAAGGCTGGG TTCTCCCACA TCCCGACTGC ACCTGTCCAC ATTTCAGGCT TCATTCATGC 4260 CAGGAGCCCC AGACCTGCTC CATGCACCAG CTCCGCCCAA GCCTGGAGCC CCGGGCTGGC 4320
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