Tag | Content |
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EnhancerAtlas ID | HS048-35795 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr8:56952300-56953230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr8:56952319-56952330 | AATTGTTTATT | + | 6.02 | IRF1 | MA0050.2 | chr8:56952710-56952731 | AAAGTAAAAGTGGAAGAATAA | - | 6.19 | IRF1 | MA0050.2 | chr8:56953208-56953229 | CTTTCCTTTCTCTTTTCTTTC | + | 6.3 | IRF1 | MA0050.2 | chr8:56952628-56952649 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | NR2F1 | MA0017.2 | chr8:56953037-56953050 | CAGTTGACCTTTG | - | 6.41 | SOX10 | MA0442.2 | chr8:56952801-56952812 | TGCTTTGTTTT | - | 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 |
GH08I056040 | chr8 | 56952961 | 56953110 |
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Enhancer Sequence | ATAGTTTTTC CAGTTTCTAA ATTGTTTATT TTTATTTTTC TTTAAAGACA GGGTTTCTCT 60 CTGTTGCCCA GGCTGGAGTG CAATGGTGCA ATCAGAGCTC ACTTCAGCCC CCACATCCCA 120 GGCTCAGGCT CCAGCTTCAG CCTCCCAAGT AGCTGGAACC ATGGGTGTGA GCCACCATGC 180 CCAGCTAATT TTTATATTTT TTGTAGAGAC GGGGTCTCGC TATGTTGCCC AGGCTGGTCT 240 TGAACCCCTG AGTTCAAGCG ATCCTCCTGC CTTGGTTCCC AAAGTGCTAG GAATACAGGT 300 GTGAGCCACT GCCACTGTTC CTTTTTCTTT TTTCTTTCTT TTTTTTTTTT TTTTAAAGAA 360 GGGAACAGCT GACGTGGCAA TGAAAAGAAA ATACTTATTT TTTTTTTTTT AAAGTAAAAG 420 TGGAAGAATA AAGAAGGGAT GAGAAAAGCT CACCGTTTCT CCACACAGGC TGCAGGCTTA 480 TAGTGGCACG CTCTTATGCT CTGCTTTGTT TTGACCAAAC CAGCTCTGTA GGATGGATTG 540 ATGAACAACA GAATTTTTAG ATTCAATTAA GGAAGGTAGA GCTTTTTCCA AGGTCCTTAT 600 AGAGAAAAGG GTGTCCAAGA GTCCAAGATT AGCCTCACCA GTCACTCCCA GAATCACACA 660 AGAGAGAGCT ATCCTTAAGC CAATTAAGCC AAGAAGAGCG ATAAGTCATA CATTTCTGTG 720 GACGTTTCCA TCACATACAG TTGACCTTTG AACAACACAG GTTTATGCTG CAAAGGTCCA 780 CAATATATTG CTTGCCAGTA TATTGGTGTG TGCCTGTAAC CCCAGGTACT TTGGAGGCCA 840 AGGCAGGGGG ATTGCTTCAG GCCAGGAATT CTAGACCAGA CTGGGCAATA TAACGACACA 900 CCGCATCTCT TTCCTTTCTC TTTTCTTTCT 930
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