Tag | Content |
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EnhancerAtlas ID | HS193-35100 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr8:130697040-130699150 |
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) |
NFIC | MA0161.2 | chr8:130698399-130698410 | TATGCCAAGTA | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr8:130698691-130698706 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40042 | chr8:130697124-130698840 | K562 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I129684 | chr8 | 130696629 | 130702024 |
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Enhancer Sequence | AGCTACCTGA GGTCAGATCA TGATTCAGAA GAAACAAGTT AACAAGATTG TGCCTCTGAT 60 GGAGCCCAGA CATGGTCAGA TATGGTTTCT CACAACCTTA CATGTCAAGA GGAAAGAATT 120 CCAGACTAGA TGTCAGGAGA TCCGGGTTGT ATTCTCACCT CCTCCAGTCA CCAGCCAAAA 180 AGTCATGGCC ACATCATTCA ATTTATCTGG GCCTCAGTTT TCTAATCTAT ATATTGGGAT 240 AACACAACCT TCCCTGTCAA GCTGAATAGA TTCTAAATAG CAAAGGAAAT AATGAAGCAA 300 TATACAAACA TAAGAGACCT TTATGAATCC TACTACAGAT CCATCAGCGG TGAATTTTCC 360 AGCCCTCTAA AACACATCAA AGAATTGTAA ACAGAGAAGG AAACTCTGAG CCCAACTAAT 420 TTTAGAGACA GAGAGACTGA CTTCCTGAGA AGGTAGGCAG CTTGCCCAAA GATTCAGAGT 480 GAGTTAGGAA CCCAGCTAAC ACTAGAAGCC AGTGTCTGGA TTCACACAGG AATATTCCTT 540 TTATAAGACC ACCTTTACGG TGATAAATGT CCCAGACGCG TTCACATAAA CACGTTGACA 600 GCAATTCAGT TTAGTTCCGT TTATTTCAGT TAAGTAAAGA TAAGCTGAGC ATTTGTTTGC 660 CATGTACAAT GACCTCTTCA GTCAAGGAAT TCCAGCTCTT GTTTTTGTCT TAACTTCTTT 720 CAACTTTGAG GGTTTCTTTG CATGTTCCTT ACCTAACAAG ACCAGCCTGA AAAGAGTAGA 780 AAAAAACATA AAGAAACTTG GAGTCTGAAT TTTCCACATG CTGGGAGCTC TCACACCCAA 840 TTCCAGATAC AGCACTCTCC TGAATGTGAC CTGAAGTGGT TTCCTCAATT GATCACATCC 900 CAGGAATCTG GAGAGCTTCC AGGGCAGGGA AAATTAGTTA CAGAGTCACA GAGTGGTGCG 960 GCCTGTCACA TGAAAGTCAC TTCCAGCTTG GAACGGATTG CACATTCCTG CCTTCTGAGT 1020 GGTGTTTCAG ATGACTGGGA TCTGGCCTGT CTGCAGACAG GCCCCAAAGC AGCAGAAGGA 1080 AGCCAGCGGG CAGGGGCATT CCAACACCGT TCCCGAGACC CGCAGTCACA GGAAAGGAGA 1140 ACTTCCTGAG GCTCCTCCAA GCCTTGCCTC AACTTAATGG TGTTTGAGAA AAACATCAAG 1200 TTTCCATTTA CCTCCATTTT GAAACACTGA AAGCATTTGT CATTAAATAG CATGATGACT 1260 CTCCTGCCTC AACTCAGAGC TTTGTCAAAC TGCTCACATG GCATAAACAA GGATGATGGG 1320 GTTTCCTACA CATATATCAG AACTTCTAAA TGCTTCTTAT ATGCCAAGTA CCATTATATA 1380 CCATGCCTTG GCTCATCTAA TCCTTACAGA CAACCTCAGG AGAGAGGTGC TCTATATCAC 1440 TACCACAGCC AAGGAACCTG GGGCTCAGGA TGGTTAAGTA ACTTGTACAA GGTCAAAAAT 1500 TGGCAAATGA CAATGCACGA ACTTAACACA GATCTGTCTG ACTCCAAATC CCAGGTCTAC 1560 ACTGGCTGGA TAAATATGAG GCAGAGGCCA CATGTAGTAG CTCACGCCTG TAATCCCAGC 1620 ACCTTGGAAG GCCGAGGCGA GTGGCTAACC TGAGGTCAGG AGTTCAAGAC TAGCTTGGCC 1680 AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAACT AGCTGAACGT GGTGGTGCAT 1740 GCCTGTAATC CCAGCTACTT GGGAGACTGA GACAGGAGAA TTGCTTGAAC CCGGGAGGCG 1800 GAGGTTGCAG TGAGCCAAGA TCGCACCATT GCACTCCAGC CTGGGCGACA AAAGCGAAAC 1860 TCCATCTCAG TAAAAAAATA GGTATATATG AGGCAGAATG ACTTTCAAAT AATACACAAT 1920 GGTTTCAGAA TCTGGCCTCT GTTTTGTTGA TTGCAAGGCC CTGTCATATT TCCAAGTCAC 1980 CTATTGCTGG GTTTCACAGC TTTAATGGTT TGAAAAGTCT TCCTTATGTC AAAATGTTTC 2040 AACAGGCTTC GTTCCCGCCC TCTGCACCCC ACAGTCCTCT TCCTTCCCAA ACTCTCCTCT 2100 GAGAAGTCTG 2110
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