Tag | Content |
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EnhancerAtlas ID | HS091-36841 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:74318340-74319480 |
Target genes | |
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) |
ZNF143 | MA0088.2 | chr4:74318795-74318811 | CAGTTCATTGTGGGAG | - | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 74318749 | 74319405 | chr4 | 74318800 | 74319000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I073449 | chr4 | 74315661 | 74321126 |
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Enhancer Sequence | AGTAAGAAAC TGTTACTTGC TAGCATGGAA AAGAATGACA ACCCCAAAGA GTAACTGAGA 60 CTTCTACCTC GCTCACCTAA CACTATTGGG CTCACTAACA GAGCGTTACT CCCAAAACAC 120 TTAAAATGCC TTTGAAAATA GTTTTGTCTC AGTGTCTTCA CAGTCTCATT GGGGAAGCAG 180 GTCTAGAAAA ATTGACGAGG GTGGACAATT TCCTGTTTGT AAAAATAATC TCTGTTGTAA 240 CTGTTATTGT GATATGTATT TGGGGGTTGA GGAAAAGTGG GCAATCTATT CTGAGGAATT 300 AGAGTGTATC TTTGCAGCAA ATTTGGGTAC TTCCATTCCA AGCACAGGAA ACACATCATT 360 GAATCTTTTT TTACACTATT TACACTTTGA AGAGAATAAC CATCTTATTT AATTCAACCA 420 TGCAGTTTGG GTGTTAAGAA ATGACATGTA CATTTCAGTT CATTGTGGGA GCTCTTTTGT 480 AATGGTGATG GTCATGCAAG TCAATGGAGC TTATGTTCTT CAAACTCCCA TGCATTTTAA 540 TCCTCACTTG TTTTGTAAAT AGTCTTCCTT CATTGGAAAA CCCATTCTTC TCTTTTTTCC 600 TCTATCACAG TCTGAGGTAT GTTTCACAGT ATGATAAGAA TGTTGCCTGT TCTGGCAAGC 660 TTTTTCTATT GCTCTGGTCT ACTTTCTATT GCTCTGGTCT AAGTCCAACA TGAAAGGCTT 720 GCTAAGTGAG CAGTGCAGGC AATTAGTGCT GCCAGTGCCC AGATAAGGGG TGTGATAACT 780 GGATGGGCAG GATTCGGAGA TCTGGGTCTT TGAGTGTAGA TAAGACACAG TTAAGAAGAG 840 CGGACAGGAA AGGATATTCC TGGGGGATGA GGGGAGATTG CCTTCCACTA CACATAAGTA 900 TGGTCAAGTA TGAAATAGTG TTTTATCCAC AACCTGCACA ACTCCAGGCT GGTGGAACAC 960 TTGGCATGCT TTCAGCCTCA ATCTTTCTAC TGAAAGTACT AGACAAGGTG TGTGTGGTCA 1020 GTCTGGTGAT AGGTTGATGG AGTAAGGGTT TAGGCTCTGA AAATTCTCTA CTAGGAAGGC 1080 TGTAGAAAAA TAGCATTGCA TAACAGACTT CTCTTGTATT TTGTTTTGTT TTAAATCACA 1140
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