Tag | Content |
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EnhancerAtlas ID | HS091-20470 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:56294100-56295980 |
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) |
IRF1 | MA0050.2 | chr17:56295286-56295307 | GAACAGAAAGAGAAACAATAA | - | 6.46 | Pou2f3 | MA0627.1 | chr17:56294321-56294337 | TCTAATTTGAATAAAA | - | 6.05 | RUNX1 | MA0002.2 | chr17:56294152-56294163 | TTCTGTGGTTT | + | 6.32 | SOX10 | MA0442.2 | chr17:56295183-56295194 | AAAACAAAGAA | + | 6.62 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I058217 | chr17 | 56295241 | 56295330 |
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Enhancer Sequence | CAAAGACAAC AGAGTGAATC AAATGCTTGA GCCAAACCAG CACCACTTCT TGTTCTGTGG 60 TTTATTATAA CCAAAGTCCC TATTCTTATA TTTGCCACAA AAACTAGCTG GAATTCAGCA 120 ATTTAGTAAG CACTCAACCT AGAGAAATGC TAGAGAGGCT GTATATGAGA GTTAGTATGA 180 GTAGAAGCCA AGATTAGAAC CCAGGAAGTC TTAGTCATGA CTCTAATTTG AATAAAAGAA 240 AATACCCCCC AGGAATTTTT TTCTGGGGGG GATGGAGTCT CACTCTGTCA CCCAAGCTGG 300 AGTGCAGTGG CACTGTTTCA GCTCACTGCA ACCTCCTCTT CCTGGGTTCA AGCGATTCTC 360 CTGCCTCAGC CTCCCAAGTA GCTGGGATTA CAGGCACACA CCACCAACCC AGCTAATTTT 420 TGTATTATCA GTAGAGATGG AGTTTTGCCA TGTTAGCCAG GCTGATCTTG AATTCCCGAC 480 CTCAGGTGAT CCACCTGCCT TGGTCTCCCA AAGTGCTGGG ATTACAGGCG TGGGCCACGG 540 CGCTCAGCCC GCTCCAGGAA ATATCTAATC TAACTGGATA TAAGAAACTG AAATTTAGAT 600 ATAAGCTGAA TAGCCAGCCC TTCCTCAGTC CCAACTGTCT GCATTTGCTA GAAAATAACC 660 CTGGCATTTT TATCTTTACT ATTTCTAAAG CCATATATGT AGAATCACAA ACACTGAAAT 720 TTAGGAGACC AAGTGTAAGG AGAGGACAGT GAAGGCAAAT AAATGATTTT TTAACAGAAC 780 CAAATCTGGC TGAATGCAGT GACTCACGCC TGTAATCCCA ACATTTTGGG AGGCTAAGGT 840 GGGAGGATCA CTTGGGCCCA GGAATTTGAA ACCAGCCTGG ACAACATAGC AAGACCTTTT 900 CTCTACTAAA ACTTTAAAAA AAAATAAACT GAGTGTGAGT CTGTAGTCCC AGCTAGTTGG 960 GAGGCTGAGG CAGGAGGATG GCTTGAGCCT GGGAGACCAA GGTTTACAGT GAGCTATGAT 1020 CATACCACTG CACTCCAGCC TGAGCAGAAG AATGAGATTC TGTCTCAAAA CAAAACGAAA 1080 ACAAAAACAA AGAAAACAAA TCTAATCTAA TACACTCTTG GGTATGCCTT TTTCAGAGAC 1140 ACGTTTCACA ACCTGTGAGC CCACACTCTT GCCCAGGAAC AGCTCTGAAC AGAAAGAGAA 1200 ACAATAAAAG CAAACAGACT AGTGACCTGA CAACAACCAC TCTGTCCTCT CCTCCTCATT 1260 CTTTTGGTTT CCCAGATAAG GAAAACCACA AGAACACAGT TGATCTATAC ATGCACATCA 1320 TATGCAGATT TTGCAAGCAG TCTCCAGTTT AAAAATTGTT TTTAAAAGTG TTTATATGTG 1380 TATTTAGGGT TTGGGGCACG TTTTCTCTTT TAAAAATGCC ACAAATAGGA CGGGCGCGGT 1440 GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC GGGCGGATCA CGAGGTCAGG 1500 AGATCGAGAC AATCCTGGCT AACACGGTGA AACCCCGCCT CTACTGAAAA TACAAAAAAT 1560 TAGCCGGGCG TGGTGGCGGG CGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 1620 ATCGCGTGAA CCCGGGAGGC GGAGCTTGCA GTGAGCGGAG ATAGCGACAC TGCACTTCAG 1680 CCTGGGGGAA AGAGCAAGAC TCCGTCTCAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA 1740 AGCCACAAAT AGAATGTAGG TTGCCGGGCA ACTCTATAAC ATATCAGAAG TATAGTATTT 1800 GTTATCTCAC TACATTTGGC CACAATTCTG ATTAGTATCA TAATTAGTAT TAGATGGCAC 1860 ATCACCACCG TAACACCCAC 1880
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