Tag | Content |
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EnhancerAtlas ID | HS184-08593 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:116796490-116797600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr12:116796525-116796538 | CACATTTGCATGT | + | 6 | RREB1 | MA0073.1 | chr12:116797124-116797144 | GGTGTGTGTGTGTGGGGGGG | - | 6.17 | RREB1 | MA0073.1 | chr12:116797126-116797146 | TGTGTGTGTGTGGGGGGGGG | - | 6.38 | RREB1 | MA0073.1 | chr12:116797122-116797142 | TGGGTGTGTGTGTGTGGGGG | - | 7.19 | STAT3 | MA0144.2 | chr12:116796807-116796818 | TTTCCCAGAAG | - | 6.62 | Stat4 | MA0518.1 | chr12:116796804-116796818 | CCCTTTCCCAGAAG | - | 6.38 | ZNF740 | MA0753.2 | chr12:116797137-116797150 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr12:116797135-116797148 | GTGGGGGGGGGGG | - | 6.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_44618 | chr12:116796307-116797820 | NHDF-Ad |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I116358 | chr12 | 116796000 | 116799658 |
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Enhancer Sequence | ATTTGAGAAT CTTAAATTAT GCATGTTGTT TTGCACACAT TTGCATGTTC AATTCACATG 60 CCTGAGTTAT TCGTCTACAA GATAAAACCA AGCATAGTAA TTCAAGTAAC CTGTGTCTGA 120 TTTCTCTTCA CCCAAATTTC AGGGCTAACC GAGTTGCAGT TAAAGAATGG ATAATTAAAT 180 CACTTGGGAA GCGCAGGGGA GTGCTGGTGG ATAGGAAAGA TGGGGTTACT GAGCCAACTC 240 CTGCCTCCAT CCCGTCTGGA TTGTCAATCG TTTCTCCTTC CATGACCTGC TGGATTTCAT 300 AACCTCCACG AGGCCCCTTT CCCAGAAGGG ACTCACTGTC CTGGTTACAA TCCTTAAATC 360 TAGCTGGGCA GGAAGGCCAG GAGTGGAGTT TGTCCTCTGC CTGGTGTGGA TAACCTTGAA 420 CATAAAGAAA CCACCACAAT ACAAACGGCC CTGAAATCTG AACCAATGCC ACCGCAATAT 480 GCAGATGAGA AAGTCAGAAC CATTCCTCCA TTGGCTGACT GCCGGCCTGA CGTCACAGTG 540 GCCCAGCCCA GCGTGGCCAG AAGTGCTGTG GGCAACTTTC TGGACAAGTT GGAAAGCTTG 600 TGTGTGTGGG TGTGTGTGTG TGTGTGTGTG TGTGGGTGTG TGTGTGTGGG GGGGGGGGGG 660 TCTTTTTTTT TTTATCAGCT GGTGCTGGTT TCCTGCATTT CCTGTGTTAC GGGGGGGGAA 720 AAAGGTGTTT ATGTACAGCA AGAACTGATG AACTCAGGGC TGAAGAGCAT TTTGTTCTCT 780 GTGGCAGCTC TATCCCTTTC CTTAGGGGAG ATCTATGTTA GAAACAAAAA TGTCATAGGG 840 GAAGGTTGTG AATTCTAAAT GAACTGTGGG GACCTCACGA ACCTCTTCAG CTTAGTGGTT 900 TCCAGGAAGC CCCAGGCTGA GCCAAACTTT GTGACTTAGC TGGTGTGAGT CTTTGGCTGT 960 GATCTTGACC ACAAACTTCA AGATATGCAG GCATGGGAGG CTGGGGGCCT TTTTTATTTT 1020 TCTCTACCTC ACTTTGCCAG GTTCAATGCA AAGACAGAAT CCAATCCTCT GATCTGTGAA 1080 CTTCTGACGA TTCCCCGCCC TCAATGTGCT 1110
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