Tag | Content |
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EnhancerAtlas ID | HS118-14106 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr4:54510290-54511940 |
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) |
HSF1 | MA0486.2 | chr4:54511435-54511448 | GAACATTCTAGAA | - | 7.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr4 | 54510843 | 54511210 | chr4 | 54511440 | 54511718 | chr4 | 54510705 | 54511201 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I053643 | chr4 | 54509921 | 54512126 |
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Enhancer Sequence | CGGTGGCTCA TGTCTGTAAT CCATCCTAGC ACTTTGGGAT GGGGAGGTGA GTGAATCACT 60 TGAGGCCAGG AGTTTGAGAC CAGCCTGGCC AGCATGATGA AACTCTGTCT CTACTAAAAA 120 TACAAAAATT AGATGGTTAT GGTGGCATGC TCCTGTAGCC CTAGCTACTT GGGAGGCTGA 180 GGCACGAAAA TCGCTTGAAC CCAGGAGGTG GAGGGTTGCA GTGAGCCGAG ATCACGCCAC 240 TGCACTCCAG CCTGGGCAAC AGAGTGAGAG TCTATCTCAA AACAAAACGA ACAAACAAAA 300 ACAAAACAAA CAAAACCCCA AAACAAGAAA TAAATGTAAA GTGACTTAAG CTAGACTGAT 360 GTATTATATA TTGAAGTATT TATGTACCTG TGTTGACATA TGCTATATGT TAGTTTGCAG 420 TCCATGATAA GAAATTTACA CAATGAAGTT TATCAGAAAA CACACCACTA GCTGGGACTC 480 TCATAGCAAA TACCTGGGAA CTCATAGGCT GTCCTATTCC AGGAGGGAGC GGGATTCCAT 540 GTCAGGTGAC TTGGATAGTG TCCCAGGTTG GGTAGGTTAC CCCAGCACCA GCAGGGCCTC 600 CTTGCCAGAT GGCCAGGCAG AGACTGGGAG GTTCCTGCTG GAGGGAGCTC AGAGTATATC 660 TGGAAGGTCG TTATTACCAA CCCAGAGAAC CAGTTTGGTG AGGTTGGCTC AAAGGGCATA 720 TTTAGTCAGA GTAAGGGAGA GATGTGGTAA CAGGGAGGAG GAAGTCTGGG TAAGGATTAC 780 AAGTAGCACA GTCAAAATGC GCTTCTCAGT TTTCAACAGA GTGAGGGAGA AGTAGTACCT 840 TAGCCCCAGC CCTGAGACCT AACTCCTCAA TTCTTGCCAA CAGCAGGAGA GTGAGCCCAG 900 GAAATCTCCA GACAGCCAAA AGATGATCCA GGTGATAAGG GCACAGCCAG GCAGTGTCCA 960 CGCCAAAAAA GAACAGAAAG TTTGGCTTAA CTCTATTTTT GCCTGTGTTT TTCTCCTGGG 1020 GCAGGAGTGT AACCTAAAAA CACTCCGGGA TACACGGTGG CCCTTACACA AATTAAGAAT 1080 CCAGAGGAAG GGCTCCTTTG GCAAGGGAAC TCTCGGGAGG CTGGAGCCAT GACAGAGCTC 1140 CCCAGGAACA TTCTAGAAGA CAGGCTAGAT TTCCTGGCCT TTGGTCACCA GCCTGGAGTT 1200 TGGCAGAGCC CTCTTGTGCA GAGGGTGAAT GAAGATATTT GGTCATTGCC TTCCCTGCTG 1260 TGGGCTGTTC TCAGCATTAA GTTGTCAGTG TGCACTACCA TTGGGGTTAC CCAATGGGGT 1320 CTATTCCAGA AAAGGGAAGG TGGATTTGCC TACTCAAGCC CAAAGAGCAA GGGCCACTGA 1380 AATTGCCTTC TGAGTAATAG GATTGGCAGA CATTGAGGCA CGTTGCAAAG AACTGTTAAT 1440 TATAATCTTT ACTTTCTCTC TAACCAGCTC AGAAAAGAGC TTTATGGGAG GAATATAGTT 1500 TGAATGAGAG GCATTCTGTT CATTCTCCCA AATACTCTGT GGATTGAGAT CAGCAGGAAC 1560 AAGGGGTCTA CACTGCATTA TCTTGGCCTC TCACATGACC ACCTTCCCTG AGTTTAGTTT 1620 AGGTGAAGTA TGCCACTAGA AAAAAATATC 1650
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