Tag | Content |
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EnhancerAtlas ID | HS122-00042 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:9338020-9341870 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr1:9339393-9339408 | GGAGAGCAAAGTTCA | + | 6.3 | IRF1 | MA0050.2 | chr1:9338285-9338306 | AAAATAAAAATAAAAGGAAAT | - | 6.05 | KLF16 | MA0741.1 | chr1:9340448-9340459 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr1:9340466-9340477 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr1:9340484-9340495 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:9340448-9340458 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:9340466-9340476 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:9340484-9340494 | GCCCCGCCCC | + | 6.02 | RARA(var.2) | MA0730.1 | chr1:9339757-9339774 | AGGTCATGCAGAGGCCA | + | 7.09 | REST | MA0138.2 | chr1:9341495-9341516 | GGCACTGTGCCTGGTGCTGGG | - | 6.31 | SNAI2 | MA0745.2 | chr1:9341181-9341191 | TGCACCTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr1:9341728-9341749 | GGAGCAGAAAGATGAGGAAAG | + | 6.18 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_00563 | chr1:9337903-9340328 | Adipose_Nuclei | SE_23490 | chr1:9337921-9342330 | Colon_Crypt_1 | SE_23818 | chr1:9337980-9341807 | Colon_Crypt_2 | SE_24876 | chr1:9337785-9342445 | Colon_Crypt_3 | SE_45049 | chr1:9340486-9342190 | NHLF | SE_50208 | chr1:9338047-9342398 | Sigmoid_Colon | SE_52461 | chr1:9338392-9340456 | Small_Intestine | SE_65576 | chr1:9339233-9340062 | Pancreatic_islets | SE_65576 | chr1:9340212-9341781 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 8 | Chromosome | Start | End |
chr1 | 9338754 | 9338968 | chr1 | 9338915 | 9338965 | chr1 | 9340275 | 9340412 | chr1 | 9339070 | 9339810 | chr1 | 9338560 | 9338691 | chr1 | 9338710 | 9338805 | chr1 | 9339431 | 9341286 | chr1 | 9340488 | 9341044 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009278 | chr1 | 9338461 | 9342291 |
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Enhancer Sequence | AAACCGCGCC CATGATTCAA TGACTTCCCA CCGGGTCTCT CCCACAACAC TTGGGAATTC 60 TGGGAGCTAC AATGCAAGGT GAGATTTGGG TGGGGACAGA GCCAAACTGT ATCAGCCTGG 120 TTCTAAACTC TCCCTCTCCA AGCCACTAGA TTTCCATGCC ACACCTCACT TTGATCCTGA 180 ATTTGGGCCA TCACTTGCTA TATTTCCCAG GACTCCTTTG GTTGCAAGGG ACAGCAACCC 240 AACTCGAACT AAATTTAAAA ATGAAAAAAT AAAAATAAAA GGAAATGTCC TGGCCCTTCT 300 CCTTGGAAGG CCCCAGGGGT GGAAACAGCT TCAGCAGAGC TGGGTCCAGG GACGTTAAGC 360 AACGTCGCCA GGAAACTGTG AGTTCAGCTC CCTTTGCATT CACGTTGCCA GATTGAGCAA 420 GTCAATCTTC AAGATGCCTA GTTAAGTTTG AATTTCAGAT AAAGAACAAA TACAGTTTTA 480 ATATAAGTAT GTCCCTTGCA ACATTTGAGA CATACTTATA CTAAAAGTTA TCTGCTGTTT 540 ATTTGAAATC CAAATGTGCC TAGGTGTCCT CTGTTTTATC TGGCAGCTCC ACCGTCTGTA 600 TCGGCCATTT TCTTGCCTCC TGCATTTGGC TTTTCTTGTA AGGGAAAACG GCTCCAAGTA 660 GCTCTCAGTG TCTTGATGGC CCAAGATGCC AGAGGAAGGG AGGCCATCGA GCTGCATGGC 720 TGCACCTTGT ACATCCTAGG GAGGCCCTGG CTGGGTCTGT CGTGGATGCC GTGGCTGCAG 780 CATTGGGAAG CCCCTGGGGT GCCTTCTCAC TTCCCCCAAC ACCAGCAGCC TCCTCCCTCC 840 TCCACCAATT CTTGGGTAGG ACTGGTTGAG AGTTTCTCAG TCTTTGTCAA GGGCTGTGCC 900 AAGGCAGTTT CAAGCCTGGC TGTGCTCTCT CTTCCAATCG GATTCTGCCC AGAGCCCCTC 960 CCCATGGGGA TTCTGGTAGG GTTCACGTCT GAATCGATCA CTTGCTGGAT TGGGATGGGG 1020 GCCGGTTGTC CATCCCTGGA GTGTTGCACA GCCCTGGGTG GGATGCTCCC AGAAGGAAAT 1080 GCTGAGCACA GAACCACACA TATCTGTGCA GGGGCTGGAG GTGAAAGTTC CAAGGGATCC 1140 CGGAACTTGT CACTAAGCGT CTACCAGGCC ATAGAAATCA GGACAGCCTA GTGAACAGAA 1200 AAAACAACTT TAGCAGTTGT GATTCCATGT TCCAGGGAAG GGAATATCCA CCCAAAAGTT 1260 TTTCTAATCA TAAAGTTATT TCAGAAGCAA GTCATGCCCC AAGAAAACCA CACCGAGGGG 1320 TGTGTTTATA ACCAGAGCCT TACAGGCAGT TGGCTCCAAC GCCCACCTGC ATTGGAGAGC 1380 AAAGTTCACA GGAGACTGAG GTGGGAGGGG AAGAAGCCTC TTCCTGCTCT GAGAATCCGC 1440 ATGGGTCGCA GTGCTTCCCT TCCTCAGCTC CCCCACCGCA GGCTGCTAAA ATGACCCCGA 1500 GTGCCTCAGA AATCTCAGGG CCACCGCAGC CTCTCCCCTC TCAGCCATGG TTCGATTCCT 1560 CATAAATATT AAGACTTCAT GTGCTCCTGC GTGGATTTTC ACCAAGTCCT AAAATGCAGT 1620 GTAGACGCTC CAGGGAAGAG GAAGCAAGTG ACATTCCTGG CCCGCTCTTA CGCCACGAGC 1680 TCTGCAGACG CCGAAAGGTT GCTCACAGGA GGCGGAAAGT GCCAGGGGTT GGGCCTGAGG 1740 TCATGCAGAG GCCAACTGTG GGCCGGGGTC CCAGCGGCAG CCTCCCCACC GAGGGCTGTG 1800 TTGAACCCTG GAGAGAGAGG GCGAGAGAGA GAGAGCGAGA GAGAGAGAGA GAGAGACAAA 1860 GCGAGCGAGA GAGAAAGCTA GCATGAAGGC TTGTTGGAGG CCTGACTCCC CAAGGCCAGA 1920 CCCTAAGGCC TTGAAGGTCA GCCAAGAAGT TGACCAAGCC AAGAAGTCCT GAGACTTGGA 1980 GCCACAGGGC CAGTGGGGCA CCATCTCCCC AGAACAAAAA CTGTACCCCA AGAATTGAAG 2040 GGAAATATTA TTTTTACTCT GAAACGTTCT GGAGCAGAAT GCAAAATTCC ATCCCTTTCA 2100 AATAGAAAAC ACAAGCTATT CACACTTGAG GTGGGTGAGG GTGCTTTTGG GGAAAAGTTT 2160 GAGAGTCGCG TCCTGGGCAC TGGGCAATCA TCAGAGGGTG TCTCCCTCGG GAGGGGTCCA 2220 GTCAGGCCTG GCTTCACGGG GATGGTCAGT GAGGCAGGGC TGGGCGATGG GCGCCGGCTC 2280 CTCCTGGAGT CAACCTTTCA TTCATTCATT CATTCAGCAA ATGGCAGTCG TGGGGTAGGC 2340 AGCCATGCAC ATGGCAGTCA AGGCCCTCCC TTTCCATTCC AGACTGTGAT TGATCCGTGC 2400 TCCCCTCCCC GCCCCGACCC CACTCCCCGC CCCGCCCCCA CTCCCCGCCC CGCCCCCACT 2460 CCCCGCCCCG CCCCCACTCC CCGCCCCGCC GCTGGCAGCG GGCAAGGACC CACGACTCAT 2520 CCCATGGCCT CCCTCTGGGT AAGTGCTTGT CGACTGAGTC AACGACTGAA TCAGCCGCGG 2580 TTGTCAGGGC TCAGCTGGAC TGAGCGCTGC TGCCTGTGGG CGTTTCCTCC TCATGTGTTT 2640 TTTATCAGCA GCAGCGGCTG CAGGGTCCCC GTGCTCAGGG GTTGCCTCTG TCGTGCTCAC 2700 TCTGCCCCGC GCTCTGTCCA CACCCCTGCT CCATCCAACT CGCAGATGGA GCGGTTTCCT 2760 TTGAGCCCCA GTCCTGTCCA AACACACATG GGTGCTGGGC TTTCCCTGTG GCACATTTTC 2820 TACCCTCTGT AGGCAGGAAA GAGCAAGCAC ATGGAGGCAG CCCTGTTGTC CTTGGCCTTT 2880 CCAGGACACC TGGGAGGAGA CAGCACCCTG TGAGGCTAAG AGCTGGACTC TGGAGTCAGA 2940 AAGGTCTGAG TTCAAATCCC ACCCCTGCTG CTGAGAGAGT GGCACAGGGC AGTTTCACCA 3000 CTGTGAGCTT GTTCCTCCTC TGTGAACTGA ATAATAAACC CTGCTTTCCA GAAAAGAGGC 3060 GCACAGAGAG GACTTTATCA TAGGGCCCAC GATGAGCTCC CGGGGTCCGA GCGAGAGACC 3120 CGCAGCACCA CTTGGTGGGG GCAGGGCCGT GTGTCTGCAT GTGCACCTGT TCATCTGCCC 3180 ACCGCAGGCT CTCACATACC AGGGCTTTGT CTTCTGCAAG GATGACCAAG ACATGGCCCT 3240 GCACTCAGGA AATGACAGGC AAGGAGCGTT CTCAGGGGTG GCAGATGTAG CGAGAGCACT 3300 TGGGTCGGAG CCACAGGGCT CTGGGCAGAG ACTGCGGTTC CGTGTTGGGG GAAGGAGGTT 3360 AGGGAGTCAG GAAAGATCTC CATCATGTGG GGGCCTTGAA TTAGAAGTTC AGCAAGTGCC 3420 ACAGACTGAT TTCACATCCC ACCACAAGTA TTTATTGAGC ACCTATTGTG TAATAGGCAC 3480 TGTGCCTGGT GCTGGGATAC ACGGGGTGGT AGCACAAAGG AAGACACTGC CCAGGGCTCC 3540 TGGCCTGGCG GGGACACAGA CAAGGGCCCA AGGGATGGCA GCCCCAAGGG GCAGGGCCAA 3600 GCTGGGCCAT GCGGAGGGTG CCGTGGGACT GCCTGGCAGG AGCATCTGTC CACCCTGGGG 3660 ATCAGTGCAG AACGTGATTC CATCCTGATG GAAAAGACGT TTCGGCTGGG AGCAGAAAGA 3720 TGAGGAAAGC GCTGCTGTGT GGCATGGGGC CAGCTGCTTC CCCTCCCTGA GCCTCGGTCT 3780 CCTCACCCAC AAGCGGAGGG ACTTGGAGCT CTGCTCTCTC AGGTTCTGGT GGCTCTGATG 3840 GGATGTGACA 3850
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