Tag | Content |
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EnhancerAtlas ID | HS184-01928 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:181086380-181087570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:181086992-181087003 | GGGCGGGAAGG | + | 6.62 | NR2C2 | MA0504.1 | chr1:181087327-181087342 | TGACCTCTCACCTGG | - | 6.43 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_08346 | chr1:181086272-181089071 | Brain_Inferior_Temporal_Lobe | SE_26792 | chr1:181084944-181089552 | Esophagus | SE_33995 | chr1:181085695-181089584 | HCC1954 | SE_35128 | chr1:181085943-181089307 | HeLa | SE_36287 | chr1:181086167-181089589 | HMEC | SE_37490 | chr1:181086153-181087846 | HSMMtube | SE_42499 | chr1:181086053-181088843 | Lung | SE_43486 | chr1:181085722-181089458 | MCF-7 | SE_50619 | chr1:181086256-181087510 | Sigmoid_Colon | SE_62708 | chr1:181056001-181122958 | Tonsil | SE_63411 | chr1:181057191-181103433 | NCI-H69 | SE_65054 | chr1:181086221-181087719 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I181117 | chr1 | 181086149 | 181089486 |
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Enhancer Sequence | CTGAAGGCAG AGCTGGAAGG CTGTCATTCT CAGACAATTT TCTGGAAGTC TGGGTGCTTT 60 TTTCACCCAT GAAGCTCGGG TTGGCAGCTC ATAAACCAGG GAGTTCCCAG GAGAGAGAAG 120 CTAGTGGGCT GGCTTTATAG ACTCCTATGC CACCTCTCTC CTTGGCTTCA TGACACTGGA 180 TATTTGAATT CCAATTGTCC CCTTCTGGAG ACCAGCAGGG GTGGAGGGTA GGGAGCTTAA 240 CCTTTCAGCT CCACATCTAT GCCTTGTCCT TAGCCTGGCC TTGAGAGAGC TGCTCAGAAA 300 GAAGGGCGGT GAGCAGGCCA CTGGCTTTAG GAAGGAAAGA GAAAAAGCCC AGCATGCTCT 360 TAGAAGACCA GCATTCCTGC CTCCCCAAGC ACTATCTCTG GCTCTCCTGC CACTGGACAC 420 CTCTACCCTT AGCCAGGCCA AGGGTGTGTG CCCTGAGCCT CACTCACGTC CTTCCTCCTT 480 AAGGGCCACT CACAGCTTTG GAGAGCAGCT TAAGTGGCAG AACCGGTATC AGAGCACCCC 540 GGGGCTCTGT GAGGCTGTAG CTTCTACTCC TGGGAAAGGC TGGAGGCTAT TTCTACTCCC 600 TTAGTCAGCA CAGGGCGGGA AGGGTGAGGG CCTGGGAAAG GCCAGTGGTG TGAGCTTCTG 660 CAGTAATTGC TCCTCTGTAA ACACAGTAAT AGCAGGTCTG GGATTATGGC TGTTACTCCT 720 GATAATTATC AGCTGCAGTG CCTTCCTCCC TAGGTGGGCC ACACGAGCTC ATCACAGCAC 780 AGGGGGCTGT GGAGTAAGCT CCAGATTTCC CAGATCTCTT TCTACAGTTG CTAGGCAACT 840 AGGAGTCTGT GCTGGAAGCA GGGGATCTCA TTTAGGAAAA TCTCCCTAGG TCCCCCAAAT 900 CTCTGAACTC GAAATTGATT GTTCTCCAAG TGGAGGCCTT GAATGACTGA CCTCTCACCT 960 GGGAAGGTCA GAGGCCCGTC CAGATGCAAA GGCAGTCCGT CTGGTAACTG AATGAGGGAC 1020 CCAGCCAGCC CAGGGCACAT GGGGAGGAGA GGCTGGTCTG GGAGAAAGCC TTTTGCTGAA 1080 TCCCATGACT TGTTTAGGGA ACGGGGCTGG TTCCTGTGTA CTGTGGCTTA GCTGGCTGGG 1140 ATGAGAAGCA GCTTACAGGT GTCCACCTTG TACTGACCAG AGAAGCCTAA 1190
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