Tag | Content |
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EnhancerAtlas ID | HS184-21612 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:172313110-172314380 |
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 | chr3:172313533-172313554 | GAAAAGAAAACAAAAGCAAAA | - | 6.21 | IRF1 | MA0050.2 | chr3:172313539-172313560 | AAAACAAAAGCAAAAGCAAAA | - | 6.47 | IRF1 | MA0050.2 | chr3:172313997-172314018 | AAATAGAAAGTAAAACTGACA | - | 7.15 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25411 | chr3:172312002-172315855 | DND41 | SE_29546 | chr3:172308272-172314754 | Fetal_Intestine_Large | SE_33824 | chr3:172312040-172314887 | HCC1954 | SE_49845 | chr3:172313020-172315690 | RPMI-8402 |
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Enhancer Sequence | CCCGGCCCAA CATGTCCGTA TTCTCAAAGC TATAGAGGTG TCTTTGCTAT TTTGTTCTCT 60 TAGGTAAGAA CCGGGTCCTC ACCTTACACT TTATTCCTCA GGTGAAGAGA CTCTGTGTGT 120 GTCCATTCAG GGAAGCATGA GAGCATTTGA TTTCAGCTGA GCAGGTTTAG TCATCTAGGA 180 GCTGCTCTCT TAAGTGTTTA ACACAATCGT TAACTAACTA AAACTTGCAG GAAATTAATC 240 TGGAATTTCC CAGTAATTAC ATGTTTTAGA TAAGTTTTTG AATTGAGTCC AAGATGATGT 300 GATAGTGCAT GTTCATAATT AACTAAGAAA CTGAGAAAAG CTTTCTTAAT CTAAAAACAA 360 AGCCAAAAAT CTTTCCATGC AAGGAAAGAA AATCTTAATT GATTAACTCA TTAATAGAGC 420 AGGGAAAAGA AAACAAAAGC AAAAGCAAAA AAACTAACTT GAGATATAGC TGAACTCATA 480 ATGTGTATTT GTTTTTATTT CCAGTTGCTG CTTACCATTA GCTGTGCAAG ACCAAAGGAT 540 TTTGTGCTTT CTCTTGCCTA GTAATTGTTC AGTCCAAAAT TTAACCATGT TGTTTTTGTG 600 TTATTACCAG GAGCAAGAGG ACATGTGTAT TGGTGAGAGA AGAGGGGTGA GGAGTCAGGG 660 ATAAGATGAA TCTGATTAAC TTCAGGGGTT ATTAGAATAA ATCTTGTAGG CTTGGAGAAT 720 CTTGTAGGCT TGGAGAATCT AGAGTTCTAT GAGAAATGGT AAGCAGACTT CATAAATCCT 780 GTCTGCGTTG CTGCTATGAT CTTGGCCTTC CCCTGACATA CTCCCAAGAA ATAGAAACGA 840 ATAGAAATAG AAATCTAATA GAACTAGAAA TAGAAATATT TCCCAAGAAA TAGAAAGTAA 900 AACTGACAAA GCCAATGCAA AGAAATCAGT TCGGAAGCTG TTAATTTTCA CACGATCTGT 960 GTTCAGTAAC CGCCCTCTAT CGGCTCTCCT GAATAGCACA CTATATGGGA CGGAGAATCT 1020 GAAAGGCCTT TTTGCTGGTT TTCTTACTAA CAGAGAGTTC ATAAACCAGG ATCTTCTTCA 1080 GCCTCCAAGG TAAGGAAATG TGTGATCTCC AAGCTCCCTC TTGTATGTAT TGTGAACGCC 1140 ACTGTCAGAA GAGAAACACC AAAGTTATTC ACCTGGAAAT GTTGCAGTAT GAAGACCATG 1200 TATTTGATGG AGAGGTTATT TAAATGGTAA CTTTGTTAAT GAATTTCTTT GCTAACTTTC 1260 CCTGCTTTAT 1270
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