Tag | Content |
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EnhancerAtlas ID | HS048-20298 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:47149730-47151330 |
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) |
Hnf4a | MA0114.3 | chr2:47150596-47150612 | AGGGTCAAAGACCAAA | + | 6.07 | ZNF263 | MA0528.1 | chr2:47150399-47150420 | CCTTCAGCCCCTCTCTCCTCC | - | 6.38 | Zfx | MA0146.2 | chr2:47151118-47151132 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH02I046922 | chr2 | 47149166 | 47150885 |
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Enhancer Sequence | TCTGTGCATC TCTGCAAATT TTGTTTCTGG TTCATATGTA CTTCAATCCC TGAAGGTGTG 60 AGAGGTAGAA ACCACTCAGA GTTTCTCCCA TTCTCTCACT CAACAACAAA AAACACGGAA 120 GACATCTCTA CCAAAATGTG GGGAGGGGCG GGGGGCTCTT CCCACACTGG AGGAAGCACA 180 TCAATTCTGC AGCAGACACC AGCTGGGAGG CCTCCAATTC AATTCAATTC TGATGCCATC 240 TACCTAGAGA TAACCTCAGA AACCGCAGGT TGAGGGTTCA GTTTTACAAA ACAGCCCTCT 300 CTTTCCCACC AGTCGCAAGT CCAAGGCCCC TAAAACATCT GACTGAATAG CTTTTAGATG 360 GATTTCCCAA GACCCCCTCT TTATTACAGT TTATTACAAA GGCTATTTTA AAGTATACGA 420 ATAAACAGCC AGATGAAGAG ATACATAGGG TGAGGTCTGG AAGGGTCCTG AGCACAGGTG 480 CTTCTGTCCC CATGGAGTTG GAGTGCACCA CCCTCCTGGC CTGTGGATGT CTTCTCATTC 540 ATCTTCCTGT CAGCCTCCAT GTGTTCAGCT CTCTGGAAGC TCTCCAAGCC CTGTTATTTT 600 GGATTTTTAT GGAGGCTTTA TTACATAGGC ACAGTTGACC AAACCATTAG TCATTGGTGA 660 TCAACTTAAC CTTCAGCCCC TCTCTCCTCC CTGGAGGTTG GAGGTGGGGC TAAGAGTCCC 720 AACCTTCTAA TCACACCTTG GTCTTTCCAG TAAAGAGCTG TCATTCTGAA TTACCTGGGG 780 GCTGCCAGCC ATCAGTCAAC CATTAGCTTA CAAGAAGACA TCACTGTGGA GTCTTTAAGG 840 ATTGTAGGAG TTGTATGCTA GAAAACAGGG TCAAAGACCA AATATATATT TCACAATATC 900 ACAGAAGGTA TAGGCCTTGG AGAGTCCTAG CCATATGTGA AAGTATCAGA CCTGTCTCTT 960 TACTCTTTTT AACACAAAAT TTCTTCCCTT GTTGCAGTCT CCATTAAAAC TCAGAATTGA 1020 CCAGGTGTGA TGGTTCATGC CTGTAATCCT AACATCTTGG GAGGCCGAGA CAGGAGAATC 1080 GCTCAAGTCC AGGAGTTTGA GACCAGCCTG CACAACATAG GAAGACCCTG TCTCTATAGA 1140 AAAACTTTTT TTTTTTTGGA GACAAAGTCT CACTCTTGTC CACCAGGCTG GAGTGCAATG 1200 GCGCCATCTC AGCTCACTGC AACCTCTGCC TCCCAGGTTC AAGCAAATCT CTTGCCTCAG 1260 CCTCCAGAGT AGCTGGGATT ACAGGCGCCT GCCACCACGC CCAGCTAATT TTCTTTGTAT 1320 TTTTAGCAGA GACGGAGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTCAG 1380 GTGATCCACC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACTGTGCCC 1440 GGCCTATAGA AAATTTTTTA AAAAATAGCC AGGCGTGGTG GTGTGGGCCT GTAGTCCAGC 1500 TACCCAGGAG GCAGAGGTGA GAGGATCGCC TGGGCCCAGG AAGTCAAGGC TGCAGTGAGC 1560 TATGATCCTG CCACTGCACT CCAGTCTGGG TGACAGAATG 1600
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