Tag | Content |
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EnhancerAtlas ID | HS091-41576 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:70490450-70492920 |
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) |
Hnf4a | MA0114.3 | chr6:70490922-70490938 | TTTGGACTTTGTCCTA | - | 6.1 | IRF1 | MA0050.2 | chr6:70492811-70492832 | AAAAGAAAAATGAAACTGGAG | - | 7.05 | LHX2 | MA0700.1 | chr6:70492731-70492741 | ACTAATTAAC | + | 6.02 | Mecom | MA0029.1 | chr6:70490622-70490636 | GAGATAAGACAACA | + | 6.16 | NFAT5 | MA0606.1 | chr6:70490943-70490953 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr6:70490943-70490953 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr6:70490943-70490953 | AATGGAAAAT | - | 6.02 | Nkx3-2 | MA0122.3 | chr6:70491307-70491320 | ATAAACACTTAAA | + | 6.71 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I069779 | chr6 | 70489259 | 70491955 |
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Enhancer Sequence | GATAAAAGGA AACAATAGAA ATATTAATGA AACACCCATT TGCCTAACAA TTAAAAGTCA 60 AGTTTTAATA CGACTGAATA TCACTTCCAA AATCTATCCA CCCACATAAA AACAATCTAT 120 GTCTTCAATA AGTGAGAGAC AGACAATAGA CAAATTTCAG TATGTAAATG CTGAGATAAG 180 ACAACACAGT TCTGGGAAAA CACAGACAAA AGGCACCTAA CTCAGACTGA AGATGAGGAA 240 TGGCTTCTCA AAAATGACTA AACTGAGACC TGAAAGGAGG GAGAATGATC TCAGGGAAAC 300 AGAAAATAGT AGGAAGGAAA GAGGGAGTAA AGAACATACA CAGAACGTTT GAAAAAAGCT 360 TCAAGAAGCT AAATATAGAT TAAATTGAGC TTTTGGAAAG GTAAGAGAAA CCAGGTGGAG 420 AGAGGGAAGA GAAGGACACA TATGTCAGGG GCTTGTGAGT CATGCTGAGT ACTTTGGACT 480 TTGTCCTAAG GGCAATGGAA AATAGTGATG AATTTTATGC AGAGAGCAAC AAACCTGATT 540 AGTACTTCAG AAAGAACATA TTTGAGCATA TTATACATTT TTTTAAAAAC CTACAGGAAA 600 AATCAGTCTA ATCTCCTTTG CATTCATCCC ACACAAGGGT TGTTCGAATT ACTAAGCTTA 660 GAAAATATAA TTCAAATTAA TCTTTTCCAA TAGAAAAAAA ATCTATACCC TATTCTGTCA 720 GAACTAAGGT ACAATGTCAA GCCTTTTTGG CCTATACTCT AAATTCTGTG CATGTGAAAA 780 ATTAAACGTG GAGAATCTAA AGGACTTATC ACTGCTATTA AGTATAAAGC AAAATTTAGA 840 ATCCAGGTCA GTGTTTTATA AACACTTAAA GAGCTCAAGT CAGTGTCAAC ATTCTATGAG 900 TGCTCTTAAA AAAGGGCATC AATATTTAAT TCTCTTAAGA TAATTAAGGA TTTTTCTTTT 960 CTCTTTTTTT TGCCCATAAA CACCTCTAGC AATGAGTAGC TATAAATTTG CTGATAAATG 1020 CCTAAAATAT AAAAAAAGTA GAAAATCCAA ACTTACTTCT ACAAAGGCAA AACCTTGATA 1080 TCCAAAGCAC AATAAAAACA ATATGTTCCC AATAGTAATA AGGAATAGTA ACAAACCCTT 1140 AATAGGCCAA ATAGAAACAT TTATGTTAAC CATATAAAAA ATAAATCACA GGATATAACA 1200 AATTTAATAA ATGGAAAGTC ATCTGTTCCC ACATTTAAAG ATTGTAAATA CCAACTGCCA 1260 TCCAAATTAA TCTTAAAATT AATATATATC ACCAATCAAA ATCCCATTGT GCTAGGAGGT 1320 AGAGTATATT AACATATTGA TTCTAAAAAT CATCTGACAA AACAAGCTAG GGCCAGAAAT 1380 AAATTTGAAA AAGACCAACA AGAAGGAATT TCCCAATTAC TATCCTTTAC TAATAAAACG 1440 TGAAAATCCA CTATTATATA ACCTTTCACC TACCTATTGG CAAAATTTAA AACAATAACA 1500 TCCAGTAATG CCAAAATGTG GAGGGAAAGC CATCTGCTAC ACAGTAAGAT AGTCTACCAT 1560 GTAGACATTC TTTATTGAAT CGATCCTAAA AATATTCACA CAAATTAGGA TGGATATTAG 1620 TACATAGATA GTTTATTCAT TGGACAATAC TACTTGTCCA ACAAATTACC TCAGGAGCTC 1680 TTACAAAGCG ATAAGCTAGC CCAAATGGGC CCTTCCTTTC CCACACAGCA GGAGCTGTAC 1740 CAAATTCCAT CACTCATTGG ACTAAGAGAC CCAAAGTCTC CAGGTGTTCA GCAATTGTCC 1800 TAGCATTCAG TGAACTACTT GTACCTACTC AGCTCATATT CTTTGGCACC CAAGTCCAAG 1860 GTGTTTATTC TACCTGCAAG ACCATTCTTA AGAGGCCAGG TGCGGTGGCT TACATCTGTA 1920 ATCCCAGCAC TCTAGAAGGC TGAGGCAGGT GGATTGCTTG AGGTCAGGAG TTTGAGGCCA 1980 GGCATTGTAG TACACACCTA TAATCCCAGC TTCTTGGAAG GATGAGGAAT GAGAATTGCT 2040 TTAACTTGGG AGGCAGAGGT TGCAGCGAGC CAAGATCATG CCACTACACT CTAGCCTGAG 2100 CAACAGAGCA AGACTCTGTC TCAAGAAACA AAAAAAAAAA GAGAGAGAGA GAGAAAAGAC 2160 TAGGAGGTTA TATGCCTCTA CTAAAGCACC TGCACTGTGG GAGAGTTTCT CTCTTTGCCT 2220 AATGTAGTTA CAAAAGAACC TGAGCACTTG CTGACCCTTG TCAGGGTAAA TTAGACCCTG 2280 TACTAATTAA CATTTATTGG TTTTGGGCCA AGAGTCCTTT ACCCAACAAT ATTCGGTGTA 2340 GGGTCGTTTA AAATATTTTT TAAAAGAAAA ATGAAACTGG AGACAATCTA AATGCCAGAA 2400 TAGAAATAGT AAAATTTACT ACTGTACATG CATAACATAG AATAACATGT TGACATTAAA 2460 AACAATGAGA 2470
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