Tag | Content |
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EnhancerAtlas ID | HS180-36688 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr4:78459090-78460520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr4:78459507-78459521 | GAAGAATGACTCAT | + | 6.34 | Stat4 | MA0518.1 | chr4:78459610-78459624 | CTTCCAGGAAAGAA | + | 6.22 |
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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: 2 | ID | Chromosome | Start | End |
GH04I077538 | chr4 | 78459401 | 78459570 | GH04I077539 | chr4 | 78459602 | 78460506 |
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Enhancer Sequence | ATCTTTCTTT CTGTTGCAGT TTCTAAGCTT ATAGAATCTA AGCCCAAAGT TAGAGCCATC 60 TCTGCCCCCA GAGAGTAAGA ATCTGAGAAC ACAGACAACA GAGAGGGAAG CAGAGATCAG 120 TGATGGAGAA ACTGAGTCCC AGAGTCCCAG TGGAATTGAT GGAACACCTT GAACCCACTG 180 TGCCTAAAAC CAAGATACCT CTGGATATTT TAGTTGTCTT TTTCCTACCT CAGCAATGAG 240 AAGTCTTTGG GTTGCAATGA GAGAGGAGGC AGGAAGGTGC CTCAGTTCAT GACTACATAG 300 GCTACTCTGG AAGCTTTCAC AAAAAGAGAC TGCCTCAGAG CTCTGTTTCT GCTCAGTCTC 360 ATGAAAGAGT TGTGGTTTTT TTTTGTTTGT TTTGGTTTGG TTTTTTTTTT AATCAGTGAA 420 GAATGACTCA TTATTTATCT TGAGGGTGTA ACAATGAATT GTTGTAAGAT TTATTCAATG 480 TCTTGTCTTT TTTTTTTTTT TTTTCCTACA GCTGTGGACT CTTCCAGGAA AGAAGAAATC 540 AGAAAACATC ACCTTTTCTC CACACCCACC CTCAACTTCC ACTTCTGTAC TATAGAAGCA 600 AAATTGATTA GGCTGGCTAA TTTGAAGAGA AAAAGATGAT AGGGGCTTTG TGCTTTAGAG 660 GTAGAAGAGG GTAATAGTCA GGTTCACTCT GACAAAGCCC ACTAGAGATG GTAGACCCAC 720 TGGTAGAAAT GGCTACCTGG ATACCCAAGG AGAGCATTAA TCATCCCATC TCATATCTGA 780 GCTCAGTACT GGGGGAGGGG ATAATCAGGT CTCACCAAAC CTGGCAGCCT TCCACTGTAC 840 GTGTGGGCAA AGACCAACAG CAGTGGTGTT GGTGGTGGAA GTTATCCAAG TCACATGGCA 900 ACAAGATATG TTATCGGCAG CCAATCCATT TGGGTCTGTA GCAACCTCAA TTCTTGTCTC 960 CTCAGAGGAA TGAATTTGAG GGGCATAAGG CAGAAAGAGC TCTAGGCAAG TTTTAGAACA 1020 AGAGTGAAAG TTTATTAAGC TTTAGAGCAG GAATGAAAGT GTACTTGGAA GAGGGCCAAG 1080 TGGACAGCTT GAAAGACTAG TGCACAGTTT GACCTAATTT GACCTTTTTT TTTTTTTTTT 1140 CCTTTTGAAA TGGAGTCTAG CTCTGTCGCC CAGGCTGGAG GGCAGTGGCG TGATCTCAGC 1200 TCACTGCAAC CTCTGCCTCC TGGCTCAAGC ATTTCTCCTG CCTTAGTCTA CTGAGTAACT 1260 GGGATTACAG GCATGCACCC AGAGTTAGGG TATCCTGGCT CCCAGTGAAG GGACTGGCCA 1320 ATTAATTTTA GTCATAAAAA CTACACACCC AGCTAATTTT TTGTATTTTT AATAGAGACA 1380 GGGGTTTGCC ACTTTGGCCA GGCTGGTCTC AAACTCCTGA CCTCAAGTGA 1430
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