Tag | Content |
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EnhancerAtlas ID | HS091-43806 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:50618800-50621200 |
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) |
IRF1 | MA0050.2 | chr7:50621145-50621166 | AGCTGCTTTCTTTTTTTCTTT | + | 6.15 | REST | MA0138.2 | chr7:50620863-50620884 | GGATCTGTCCATGGTACTGCC | - | 8.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 50620513 | 50620607 | chr7 | 50620655 | 50620983 |
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Enhancer Sequence | TTAGTGTCTT GAAAATATAT TGCCAAATTT TCCCCTAAAA CATGTATAAG AATGCTCATT 60 TTACCATACA ATCACTGGGC TTGAATATCC ATTTTAAGTT TAACCAGCCT TAATGATTCC 120 GTTGTACTTT TTTTTTTTTT TTTTTTGAGA CGGGGCCTCA CTCTGTCGCC TAGGCTGGAG 180 TGCAGTGGTG TGATCTGGGC TCACTGCAAC CTCTGCCTCC CAGGTTCAAG CAATTCTCCC 240 GCCTTGACCT CCTGAGTAGG TGGGATTACA GGCGCATGCC ACCATGCCCG GCTATTTTTT 300 TTGTATTTTT AGTAGAAACA GGGTTTCACC ATGTTGGCCA GGCTGGTCTC TAACTCCTGA 360 CCTCAAGTGA TCCACCCGCC TCAGCCTCCC AAAATGCTAG GATTACAGGC GTGAGCCACC 420 GCGCCCGGCC CCATTGTACT TTGACTAATG AAACTGAATA GCTTTTTCGT GTGTTTCTTT 480 GCCATTTGGA TTACTTTTTT ACTGAATTTC TTGCTCACTG CATTCTTTTC CACTAGGGTG 540 TTAGATATTT CCTATTTAAT TGTGAGAGTT CTAATATACT AATAATTCTA CTCTTACGTC 600 TGTTAAATGT TTTGCAGGCA TTTTCCTCAT TTTTGTTGGA CCCAATTTGC TTATAATTCT 660 ATTCTGACCT ATGAGAATGT CAATTTTTAT GTAGTGAAAT CTCATAATCT TTTCTTCAGG 720 ACTTGTACCT GATGTGTGAC TATTAGCAAT GCCTTTTGAA GCAAATATTC TAGCTATATC 780 TATTTGCCCT CCTGGGGGGC CACACATGTG AGGCAGCAAG CTGAAGACTC AGAAGGGGTA 840 GCTGGGAAAG ATTCAGAAAG ACGCTCAGCT TCTGGGGATA TCAGCTTTAA GTCACAGCAC 900 CAGGCCAAAG CATGTGGCTC TGGAATAAAA AAACACAACA AGCAGACACA TACCACATAC 960 ACCAAAAGAA ATATTCCTAG TCAAAGTGTA AAGTAAGACC TGGTTCTTAT ATTTTAAATT 1020 ATTCTCTGTT ATTTATTCAC AGATTATTTC CCACAAAGAC CTTTTTAGAA GGCTCTTAGC 1080 ATGAAGCCAC AGAGAATCTT GTGCTCATTT GTAGCTGTTT GATATTTTAT GCCCCCAAGC 1140 TGTGTAAATA TTAGCTGGAA GACTTAGCCT ATGATAAAGG CTGTGGCTTA TGCCTCTCCA 1200 GGCCCTTGAA ATAGCTTCTG TTGACATAAA CTGCCCAGTG TTCCAGCAGC TGCACACGAC 1260 ACTATTCTCC ACACTATTCT CTACCCCACA CTATTCTCCA TGCTGCGCTA TTCTCCATGC 1320 AGCCCCTGTG GTGCATTGCC TGTGCACGGT GAGCTGGCTG CCTCCCTGGA CTTCTGGCTC 1380 AATGTCTTTT TGCATCAGCA ACAGTCAGAG CTCATCTCCA GCCCCACACG CTTCAAGAAG 1440 AGATGGACTC CCCTGAACTC CCTCAGACCT CCTGATTGAC CTGTGGGGTT ATTTTGTTGT 1500 AATGCAACAT TTCAATAACA CCCTTTGCTA ATGGTGGGCT TCTCCAAGCA GGGTCCTCAA 1560 CTTATTTATT TTTGCATTTG CAGGACCAGT CAGGGGCCCT GGACAACAGA GAGCACTGTA 1620 GGTATTTGCT GAATGATGAA TGAATGAATG ATATTTGGTC CTCTAGACAT TTTGTTTCTG 1680 TAATATACCC TATTGGACTC TACTCTCTAC CTTTGAGACA ATTCAAATCA CCAGCCCCTC 1740 ACATATTTGC CACAAGGAAG AGTCACAGGA GACACTATGG CTCAGGAGCC ACAGCCCCTC 1800 CCACCATTGA GTCTTGACCA CTTCCACCTG TGCCATCTCC TGTCTCAGTC CCTGCCCAAC 1860 ATCTAGCCCT CCATGTTCAG CACTTGACTA AGTGTCCTGC AGTCTGGGCA CTGCAATTTC 1920 ACTCTTAGGA CTTCTCTGCC ACAGCCACTG AAGAGAATGC AGCCCAGGCC CCTAGCACCA 1980 TGGGCAAGCC CATCCACGCC ACTGTGCATG TGAGGTAGTG GATTCCTCAC AAGCCCGGAG 2040 TGGGGATGGC AACCATGCAC TGTGGATCTG TCCATGGTAC TGCCTGTTCA TGCACGCAAG 2100 ACATGATTTT GCTGCAAACA CCGGGATACT GGAGACTTTG TTCAGCCTCT CTTGACTTTC 2160 CTTTTCCATC CTGATGAAAA AAATAGGGTT GACATTTTTT ACACTATTCC AGTAAAAAGG 2220 AGCCATAGTT TATGTCTCAG AAAACACGTA AGCTTTTGGG CCTGAGGCTC TGGCTCACTA 2280 TCCCCCTCAA GCATATACTT ATAAATCCAG GCACAACACT AATTTGGCTG ATTTCCCCCT 2340 GGATTAGCTG CTTTCTTTTT TTCTTTTCTT TTCTTTCTTT TCTTTTTTTT TTTTTTTTTT 2400
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