Tag | Content |
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EnhancerAtlas ID | HS088-00592 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:15649540-15650940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:15650210-15650229 | TGGCCAGCAGAGGGCAGCA | + | 8.47 | Gata1 | MA0035.3 | chr1:15650629-15650640 | ACAGATAAGGA | - | 6.14 | SREBF2 | MA0596.1 | chr1:15650616-15650626 | ATCACCCCAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53278 | chr1:15648791-15651570 | Small_Intestine |
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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 |
GH01I015322 | chr1 | 15649495 | 15652219 |
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Enhancer Sequence | TCACCATCAG GAGAACAGCA CGGGAAAGTC CGGCCCCCAT GATTCAGTTA CCTCCCCCTG 60 GGTCCCGCCC ACAACACTTA GGAATTCTGG GAGATACAAT TGAAGTTGAG ATTTGGGTGG 120 ACACACAGCC AAACCCTATC ACCATGCACA GAGGAGGAGC TCAATAAATA AATCTCTGAC 180 AGCTGGTGCC AAAGGCCTGC TGTGTGGCAG TGATATGAAG AACAGGACTG CCAGAGCTGG 240 GGCTGGGGGC GGGGAGGCCA GTCATTGAGA GGAGGAGCCA GAACAGAGCC CAGGACAGCC 300 TCTGCTTTCG CAGCATTTGA AAAACGTCCG CCGAAACAGA AGCTGGGGTA TGTTTACACC 360 TGAGAGGATG TAAGTGAGGA AACTGAGGCC CAGCGAGCTT AGCCGGCCTT CCCGGGAAAC 420 AGCTCACTGG GGACTGGCTG CACCCTGCCA CTCAGAAGAA AGCTTTACAG GTTGCTCTGG 480 GTGTTTTACA TGAAATCTGT GTGACCCCTC TCTAGCCCCC TAATAAACCA CTTGTGAGGC 540 TGTTTCAGAA CAAAATCCTC TCATCTAGGA GAGTTTGTCT CATTTCCTGC AAGTGCCTGA 600 GCCCTGGCTC AGCAGATGCC CAAAATGTTC ATGGTTCAGA CATGAACTGA GCAGCTGCAG 660 GGTCCTGTAA TGGCCAGCAG AGGGCAGCAC CGAACACGCC CAAGCTCACC TCGAGTTGCC 720 CATTACTCGA GCAAGCGGGG GAAAATGGGC AAGTTTCCCC ACTTTAAACG CCTTCTTTTG 780 CAGGCTACAA TTCTTTACTA GCCATTGCTT AGCTCCCAGA GCAGTTTCCC TTGGTAAGTG 840 TGCTAGAAGT GGTAGCAATA AACAGTTACA ATAATAAACC CAGCAGTTAA CATTTACCAA 900 GTGCCCACGA TGGGCGGCAG TTCCTTATGG TGTTAGGATG ACTCTGTATA GTGGCTACTG 960 TCATCCACCT GTTCTAGGTC ACAACATCTA ACACACTTAT AGAGCCCTTA CGAAGCGCTG 1020 TCACTATTCC AAACTTTTTA AAATCCCCAC AATAACTCTG CGAAGAGGGA ACTAGTATCA 1080 CCCCATTTGA CAGATAAGGA CACTGAATCA CAGAGCAGTG AAATGACTTT GCTGAGGTCA 1140 TACAGCTTGC TAGGGACCGG GCTGGGATTA GAGCCTGGGG TAGGACAAAT ATTGAGCCCA 1200 GGGTGCAGAG CCCAGCCCTT TCCCCCAACG GACAGTGCCC CCCTAGCCTG GCTCCACCCC 1260 GCGCACGCCT GTGACCCCTG CCACATGGGC TGCAGCTGTG CCTACCCCTC TGGGACCCCC 1320 CACGGCCATT AGACATCCTA GAGGAATCTC CCCAGAGTGC ATTATGATCA CATTAGCAGC 1380 AAGTACTCGC TTTCATCGTC 1400
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