Tag | Content |
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EnhancerAtlas ID | HS091-48041 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:98877040-98878520 |
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) |
SRF | MA0083.3 | chr9:98878421-98878437 | TTTCCAAATAAGGTCA | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_50729 | chr9:98877894-98879567 | Sigmoid_Colon |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I096115 | chr9 | 98878113 | 98879533 |
|
Enhancer Sequence | CAGGAGATGA TAGGGAGAGC AGTGATGAGG CCCAAACAGA TAAGCCCTGC GCCCCCACTT 60 CCCAGGTCTG ATGAATGATG CCCCACCTGC CTTCACCTTC ATCCAGACTA CTGCTGGTTT 120 AGTCTTTATT TTCAGCCTCG TTAACCCCAA GGCAAGGGTG TCATTTTTCG ATTCTCAATG 180 TAACTTCTCT GCTCCGGGTT AAATTATCCT TCAATCAATG GTGTTTTTGC CCATTTTGCA 240 TAGCAAGATT CCGTGTAGTT CTGGCCTCTA AACTGCCAGA CCTATGCTGG GACACCCATG 300 CATGAAGGCC TGCTATCAAC TGAATTGCAT CCTCCCTAAA CTCATATGTT GACACCCTAA 360 CCCCCAAAGT GATGGTGTTT GGGAGATAAT CAGGTTTAGA TTTGAAGCTC GTGGTGGAAG 420 AGAAGCTAGA GAGCTTTCCT TTGCCTTCTG TTCTCCTACG AGGACACAGC CAGAAGGCAG 480 CCGTTTACCA GTCAGAAAGA GAGCCCTCAC CAGAAACTGA CCATGCTGGC ACCCTCATCT 540 TTCACTTCCA GCCTCCAGAA CTCTGAGAAA ATTAATTTCT GTTGTTTAAG CCACCAGTCC 600 AGGATATTTT GTTATGAAGC GACTATGACA GGGAGGGGAG CTGTTCCACC CCTGCTGCCT 660 CAGCCTGCAT GGCTGTCCCT GTCCCCACCT CCTCATCTTT CTATCTTCTT GCCTCTTCCC 720 TTCCCCATCT CTCCTGTGAA TTAGCTCCTT AGGGCTGCCA TAACAAAAGT ACCACAAATG 780 TGGCAGCTTA AAACAAGAGA ACTAACATGG TGAAACCACG TCTCTACTAA AAATACAAAA 840 AAAAAAAAAA AAAAAAAAAA AGCCGAGTGT GTTGGCGGGC ACCTGTAGTC CCAGCTCCAT 900 GGAAGGCTGA GGCAGGAGAA TGGTGAACCC GGGAGGCGGA GCTTGCGGTG AGCCGAGATC 960 GCACCACTGC ACTCCAGCCT GGGCGACAGA GCGAGACTCC ATCTAAAACA AAAAACAAAA 1020 AACCACCACC ACCAACAACA AAAAACAAAC AAGAGAAACT TCCTCTCTCA CAGTTTTGGA 1080 GACCAAAAGT CCAAAATCAA TGTGTTGGCA GGGCCACGAT CTCTCTGAAG GTTCTGGGGG 1140 GGATCCCTCC CTTGCCTCTT CCAACTTGTG GTGCTTCCTG GCATTTCTTA GCTGTGACAG 1200 CATCACTCCC ATCTCTGAGT CCAAGTTCAC ACGGCTTTCT TCCCTCTGTG TCTCTCTGTG 1260 TCTCAAATCT TCTCCTTTCT CTTGCAAAAA TATCTACTAG TCAATGGACT TAGGTCCCAC 1320 CCTAAATCCA GGATGATCTC ATCTTGAGAC CTTTAACTAG ATCATATCTG CAAAAATCTC 1380 ATTTCCAAAT AAGGTCACAT TTGCAAGGAC CGGGGTAAGG ACTTGGAGCT ATCTTTTCGG 1440 GGACACTTTT CTACCCTCCA CACCCACTTA CCCTTTCCCC 1480
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