Tag | Content |
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EnhancerAtlas ID | HS048-33048 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:159379290-159380630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr6:159379747-159379762 | CCAGTTCAAAGTCCA | + | 6.25 | Hnf4a | MA0114.3 | chr6:159379748-159379764 | CAGTTCAAAGTCCAGA | + | 6.45 |
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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 |
GH06I158958 | chr6 | 159379307 | 159380212 |
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Enhancer Sequence | CTTACAACAG ATGACCTGAA ACTGGATGAT TTATTCAAAA GTGGAATTTA TTTCTGACAG 60 CTCTGAAGGC TGAGAAGCTC AAAGTTGAGG GGCTGCATCT GGTGAGGGCC TTCTTCCTGG 120 TGGGAACTGT GCAGAATCCT GAGGTGACAG GGCATCACAT GATGTGCTGG CTCAGTTCTC 180 TTTCCCCTGC TTAGAAAGCC ACCAGTCCCA CTTTTGTGAC ATCCCATTAA TCAATCAACC 240 CATGAATCCT TGCGCGGGTT AATCTATTAA TGAGGGCAGA GCCCTCATGA CCCAATCACC 300 CCTTAGAGAG CCCCCACCTT TTAATACTGC CACATTGAGG ATTGAGTTTT AGAGGGGAAT 360 GCTACCATTC CACCCCTGAT CCCCCAAAAC TCATTTCCTT CTCACATTCA TTCTACTCCC 420 ATAGTTCCAA AGTCTGAACT AATTCCAGCA CAAAATTCCA GTTCAAAGTC CAGAGCCTCA 480 CTTGTGAGCC TGTGAAACCA AAACAAGCTC TCTTCTTCCA AGATACAGTG GTGGTACAGG 540 CATTAGACAG ACATTCCTAT TTCAAAAGAG AGAAATAGGC AAAAAGAGAG GAGTAATAGG 600 CCCCAAGCAA GCCCAAGACC CAGTAAAGAA GACGTCAAAT CTTAAAGCTG GAGAATAGTC 660 TCTTTTGACT CCATGTGCCA CCTGCTGTAC ACACTGGGGC AGAGGTTGGG GCCCTAAGGC 720 TTCAGGCAGC TGCCCCCACC CCCTGGCTTT GCTGGGTGCA GTCCCTGTGG CAAAGCGCCT 780 GAAGCTTTGC CATGCAGGTG CTGCATGCTG CTGGGGACTC CACTGCCCTG GGGTCCTGGT 840 GGTGGTCCCG CTCCCATGGC TCCACTAGCA GCCCTGGTGG GGACTCCCTG TAGCAGCTCT 900 GACTCCACAT TTCTGCTAGC ATTACTCTAG TGAGGGCTCT CTGCAGTGAT GCCATCCCTG 960 AACATGTCTC TACCTGGCTT CTAGGCTTTC AGCCACATCC TCTGAAATCT AGGTAGAGGG 1020 TGCCAATCCT CCGCAGCTAT TGCTTTCTGC AAGCCTGCAG AATTAGCATC ATGAGACACC 1080 ATCAAGGCTA CAGCTTGTAT CTTCTTGAGC AGCGGGCTGA TCCACACCTG GGACTACTTG 1140 AGCCACAGCT GGGGCAGCTG AGAAGCACCT CACCAGAATC TGGTTAGCAG GGTCCTGAGG 1200 TGGCCCTGGG GAGGGAGTCT GTGGAAGGTG TCTTGGGCTC ATCCCTGCCC TCATAGGCCT 1260 CTGGGCCTGT AACAGCGGGG AAGCCTCAAA GGTCTTTAAA ATGGCTTTGC GGTCTTTCTT 1320 TCACTGTTTT GAGGAGAAGC 1340
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