Tag | Content |
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EnhancerAtlas ID | HS091-36119 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:1328120-1330640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr4:1329315-1329326 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr4:1329397-1329408 | AAACCACAGAG | - | 6.14 | RUNX1 | MA0002.2 | chr4:1329480-1329491 | AAACCACAGAG | - | 6.14 |
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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 |
GH04I001337 | chr4 | 1329850 | 1330624 |
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Enhancer Sequence | AAAGCCCTGG GCAGTCCCAG ACCTGCTGCC TTCTGAAAGC TGCTGGAAGC TCAGCCTGAA 60 TTCTCCTGGT TCTCAGGCGT TTGGGGCATC TCATAATAAA TCATCATTAG GTCACGAGGA 120 TCTTCAGGGG TGGGGTCTGA GCTTCCCAGA CTGTGAGTTG GCACCTTGTT TCTCTCGCTT 180 GCTCTGGAGA GGATTTTGTT AGAAATGCAG GAAAGGCTGA CCCATACAGG GGGCTGAGAC 240 TTCGGGCCTA GGCCGGGTGG AGCATGCACC TCTCACCGGA CGCAGCCCTG CAGTGTGGTA 300 AAGAGGGAGG CAGGCAGTGC CAGCCCCAAG GCTCATCTGT TGCCAGATTC AGGGGGCACA 360 ACCGTGTCTC GTGGCAGGAA AATGGGCCCC GTTGCCATGG GTCAGGCAAG AAACAGAAGG 420 AAGCATTTTG TTCAGAGAAT GGCAGAAGCC ACCAGAAGCC CAGAGGCAAC CAGTCCTGGG 480 GAGTGAGGAT GCCAGGAGCT GTTCTTCTCA GTGAGGACCT TCTGGACTGT GGGCTTCCTC 540 CCTTGTAGAC TTTGATTTTT AGACAAAAAT GAGATTTAAA ACAGCCTTTA AAAATGTTGG 600 AGTTAAGTGT GGTGTTTACC CTAAACTGAG ACTGAGAAGC TTACAGAGAC TGATGGGTGA 660 CGTCCCCTGA TGACCACCTC CCCTCCCTCC AGGTGTGGCC GTCTCCCCCC AAGCTAGAGA 720 CTGAGCGGCC TTTCTGGGTT GATGTGAAGG TTTTTCTCTC CTGTGCTCAC ACACGCTCTC 780 TCTCTTAAGT CTAAACCTGA GGTTATTTAG GGACAGACAT TCATCAGGTT TAATTTTCTG 840 TTCTGTGATG CTTTAACCTA ACATGGACCG GTTGTTTTCC ATTTCATACA TGATTTCTCT 900 GAAGTAAGAG TTTTTACACC TAATGCTCTG AGGTGCACTC TGCACTGAGC TGTCCTTCCA 960 GCTGTGTGAG TCTATTTTTT GTCACAGTGC ACAGGTTGCA CACATTCCAG ATCATTCAAG 1020 TTGATTCACA AGTGAGTGTA GCAGAGTTAA GTCAGCACCA GCCCTGTGGC ATGTTGAAAT 1080 CAGAGTTAAG TCAGCACTGG CCCCACAGTG TGTTGAAATC AGAGTTAAGT CAGCACTGGC 1140 CCCACAGTGT GTTGAAATCA CAGAGTTAAG TCAGCACTGG CCCCATGGCG TGTTGAAACC 1200 ACAGAGTTAA GTCAGCACTG GCCCCACAGT GTGTTGAAAT CACAGAGTTA AGTCAGCACT 1260 GGCCCCATGG CGTGTTGAAA CCACAGAGTT AAGTCAGCTC TGGCCCCCAC AGTGTGTTGA 1320 AATCACAGAG TTAAGTCAGC ACTGGCCCCA TGGCGTGTTG AAACCACAGA GTTAAGTCAG 1380 CACTGGCCCC ACAGTGTGTT GAAATCACAG AGTTAAGTCA ACACCTGCCC TGCAGTGTGT 1440 TGAAATCACA GAGTTAAGTC AGCACCTGCC CTGCAGTGTG TTGAAATCAC AGAGTTAAGT 1500 CAGCACCTGC CCTGCAGTGT GTTGAAATCA GAGTTAAGTC AGCACCTGCC CTGCAGTGTG 1560 TTGAAATCAC AGAGTTAAGT CAGCACCTGC CCTGCAGTGT GTTGAAATCA CAGAGTTAAG 1620 TCAGCACCTG CCCTGCAGTG TGTTGAAATC AGAGTTAAGT CAGCACCTGC CCTGCAGTGT 1680 GTTGAAATCA CAGAGTTAAG TCAGCACCTG CCCTGCAGTG TGTTGAAATC ACAGAGTTAA 1740 GTCAGCACCT GCCCTGCAGT GTGTTGAAAT CAGAGTTAAG TCAGCACTCA TCCCGCAGCA 1800 TGTTGAAATC AGGGAGTTAG ATCAGCACTG GCCTTGCAGC ATGTTGAAAT CAGAGAGTTC 1860 CAGCACTCGT CCCGCAGAGT GTTGAAATCA GAGTTAAGTC AGCCCTTGTC CTGCAGGTGT 1920 TGAAATCAGA GCGTTAAGTC AGCACTGGCC TCACAGCGTG TTGAAATCAG AGACTTAAGT 1980 CAGAACTGGC CCCACAGTAT TTTGAAATCA GAGAAGTCAG CACTCCCCCG ACAGTGTGTT 2040 GAAATCAGAG TTAAGTCAGC ACTCACCCCA CAGCATGTTG AAATCGGAGT TAAGTCAGCA 2100 CTCACCCCAC AGCATGTTAA AATCAGAGTT AAGTCAGCAC TCATCCCACA GTGTGTTGAA 2160 ATCAGAGTTA AGTCAGCACT TGTCCCGCAG CATGTTGAAA TCAGAGTTAA GTTCATACTG 2220 GCCTCGCAGT GTGTTGAAAT CAGAGAGTTA AGTCAGCACT GACCCTGTAG CATGTTGAAA 2280 TCAGAGTTAA GTCAGCACTC ATCCCGCAGC ATGTTGAAAT CATAGTTAAG TCAGCACTCA 2340 TCCCACTGTG TGTATCAGTC AACACTTGAG GGAGTTATGC TTTGTGCTGA CCCTTAGTGC 2400 AAAGTGTGTG GGTCACTGGG GGATGGCTGT GGGCCGATGG CACCTGCTTC ACCATGGTCC 2460 ACGTTTTTAA GCTGTCCCAG GAGCTTCCCT GGGAGCATCC CCAGGACCCT CTGCTCTCTG 2520
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