Tag | Content |
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EnhancerAtlas ID | HS048-33067 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:160684960-160686000 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr6:160685892-160685902 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr6:160685892-160685902 | GGCACGTGCC | - | 6.02 |
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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 |
GH06I160263 | chr6 | 160683820 | 160685585 |
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Enhancer Sequence | CTTATTAATA TCCAAATACA GTTTGAGTTT TCTTGGGCTT TATCCTCTCC AGAAACCCAG 60 GAGTGTGTCA ACTTCTTGGT TGCATTGCTT TCTTCAAAGA GAGAGTGAAT CCGGTAGAGA 120 TAGAAAGGAT GTCCTTTACG TATCCCACAG CGGCCTCACG GAGAACGATA AGAGAACAAT 180 CATTAAAACT TTCATTGCCA TAATTTTCTG CTTTCGTTTT TTAAAAGTTT GGGTTAGCAA 240 CCAATTTCCT CCTTGACCAG GTGATTTTTT CCTTAGACTG TTTATCCAGA GCATTAAGGA 300 AAACAGAGCA TACCACCCTC CCACCATAGC TGATAAGGGG ATTCAACACA GGTGCGTGTG 360 CTAGAGTTAA GGGAACATAT TATGCTAACA TGAATCTAGA CTGACTTAAA AAATAGATGT 420 CTGAAGCAAG TCTTTTAATT CACAGCAAGG CTGTGGCTCA CCACTGGAAG TGTAACTGTT 480 GTAATCTGGC TAGAGAGGAA AGTCCATTAC ATTTTAATTT TTTTATGACT TCATTCAGCC 540 TGGAGCAGGG TGAAGTGGAT AAAAGAGAGA GTTGTCGTCT TAGAAAAATT GCTGATTTCA 600 GATCAGAAGA AGGAAATCAA CATCAAGAGC CTGGGACATT CTGTTGGGCC AAAACAAAAT 660 AAACAAAACA AGAAAGCTGA GACTATTGAC TATGTTGACA GGAATAAGGG GCCATCTGAA 720 AATGCTCCCA TTGGCCTAAA GTGGGGGAAT TTGGACATTA AAAAAAATTA ACTGCAACAG 780 ACTAGGAGTG GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCTGAA GCAGGTGGAT 840 TGCTTGAGGC CAGGAGTTCA AGACCAGCCT GGCCAACATG CTGAAACTGC GTCTCTACTG 900 AAAAATAAAT ATGAAAATTA GCCAGGTGTG ATGGCACGTG CCTGTAGTCC CACTTACTTG 960 GGAGGCTGAG GCAGGAGAAT TGCTTGAACC TAGGAGGTGG AGGTTGCAGT GAGCCAAGAT 1020 TGCGCCCCTG CACTCTAGCC 1040
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