Tag | Content |
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EnhancerAtlas ID | HS083-00248 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr1:209572230-209573450 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:209572695-209572705 | TTTAATTAGA | - | 6.02 | IRF1 | MA0050.2 | chr1:209573207-209573228 | GAAAAAAAAGCAAAAGTGAAT | - | 6.2 | Zfx | MA0146.2 | chr1:209572884-209572898 | CAGGCCTCGGCTCC | - | 6.61 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26692 | chr1:209572179-209573445 | Esophagus | SE_33755 | chr1:209567719-209574222 | HCC1954 | SE_35814 | chr1:209570058-209574133 | HMEC | SE_64219 | chr1:209569910-209574206 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I209396 | chr1 | 209570004 | 209573973 |
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Enhancer Sequence | CTTTTTCAAG CAAGCCCCAC CTACTTGACT ACTGTTTTTC AGGAGGTTAA AACAAAAAAT 60 GATGTGTCAC TTAGTTACAC AAATGAACAG CCGATTTGGA CTTTGAAAAA CTCTTAGGTA 120 TTTTGTAAAA ACGGAGCTAA ATACTAAGTA ATAAATTTTG GGAGCCAAAT CCTTCCAAAA 180 CAAAATTTCC TTGAGAATTG CCCTTCTGCG CATGGGTAAC TATTGCTCTC AGAGACAAGA 240 AATGGCTTGC TTGGATTCAA ATATGCAAAA GCTAGGTTTT AGGCATCCAC TCTCTTATTC 300 TAGAAAGATT TATTGAATAC ACACTATGTG GAAAGCATCA TGCTAGGTGC TACAATACAA 360 AGATCAAAAG GTTCAAGAGA TAGAGGCAAG CTGTCTCTAA ACTAAGATGC TGCTGGGGAC 420 CCACTCTGGG GATCTTTTTA GCCTGACTTA GCAACAGGCC ATGTATTTAA TTAGAGTCTT 480 CATTCTACTG ACGCTTCCTC CAAACTTGCA CCTTGATCAG AAGATAAAGG TCAGTCCCTC 540 TGATCTCACT GTAAGCTTTT TGGAGGCATA AGAACAGGGT CTTTGTCATT TTTTTCTCCA 600 GCACCAGATG TAATGCTTAC CCCATCCCTA AGAGGCACTC TGTCGGGAGT TGAGCAGGCC 660 TCGGCTCCGA TCACTGTGGC ATTCTAAGCA GGTGCCACTG ACAATGTGAC TCAGTTTGTC 720 TAAGCTGCAG TTTCCTCATC TGTGAAACAG AGATACTTTT GATCTGAGAA GGTTGGAAGG 780 AGGAACAAAG CAAGGGTCTG GAAGGGGCTG GCCAAGAAAC CTGTCATGCA GTCGGAGGTC 840 AGCACTTCAC GGGAGCTCCT AGTGTTAAAT GTGGAACCAC CCAATGTCCC CTGTGAGGGA 900 GCTCAGTGAC ATTAGGGGCA GACAAAGATA CTAGAATGGG AACAATCAGA TTCTACAGCT 960 AAAAAAATAA AAAAGAAGAA AAAAAAGCAA AAGTGAATTT TCTCCCCATT TCACTAAAAT 1020 AATATGCTCT AAGCCTGAGA CCTTTTCCCT CCTGTCTGCT GCCTGAAACT CATTTCTCCA 1080 ACAGAGATCT AAGCCACCAT AAATCTCATC AGGGGTCAAA ATGGCTGACA CAATTTTAAC 1140 TACAAGCAAC CACAGCAGAA ATGGCGTCAT TATTATCCCC AAGGGCTGCT CTCTGCCTTT 1200 TCTAAGGGAC AAAAGAAAAA 1220
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