Tag | Content |
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EnhancerAtlas ID | HS184-06893 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:126180190-126181620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:126180553-126180572 | CAGCCACAAGGTGGCAGCA | + | 7.03 | Myod1 | MA0499.1 | chr11:126180597-126180610 | TCCAGCTGTCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34768 | chr11:126179940-126181335 | HeLa | SE_53328 | chr11:126180027-126182312 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I126310 | chr11 | 126180161 | 126183182 |
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Enhancer Sequence | ACATCTCCAT TTGGAGGTCT CATAGGTGCA ATTCAAGAAT CCGATGCGCT AATGTACTTA 60 AAAGCACTGA GCACAATACT AAGTAGTAGC TGCTGTTATT AGTCTCATGT GCCAGGCCCT 120 ATGCCGCGTA CCGTAGCTTC AGAGATGAGT AAGATACCAT CCTTGCCCTC ACAGTCTTGT 180 TTGGGGTCAG GGGTGGGGAC ATAGTGGTGA AAAGAGGAGA GTTTGGTCAC TGCCTGGATA 240 TAAGGGGTGA GGTCCTCGAA GGTTGGAGCC ATGTCGCCCA TATTAGGTGC TTTCAATAAG 300 TGAAGAATGA ACCCACAAAC TGACCTATGT GTAGATTTGT TTTCCTGTGG GCTGGGCATT 360 CCACAGCCAC AAGGTGGCAG CATTGCCAAA ATAGTCCTGT GGCCCACTCC AGCTGTCCCC 420 TCTGTGGGAA GGCCAGCTAA GTCAGAGCCT GGGACCTCCC TCTCCAGTCC CAGCCTTGGA 480 GTCAACTCAA TGCTGCCCAC CCCGAGGGCC CTGAATGTGC AGTTCCTGCA GCCTCAGCCC 540 TCTGTCCCCC TGCATGGTTG TGCCTTTGAG TTTTTCTGCT GTCTCTGGCT GCTTCTTTAG 600 ACCTCCTTCC TAGAATACTG TTTGCCTAGG GGAGCCCCCA CCCCTCATTT CTGAGCTGGC 660 CACAGTAGAA ATCATGGGCT CAGCTGATTT TTTTCTGGTA TTCCTCTGGT CACTGGCAAC 720 TTTCTTTTCC TCTTCAAGTC TGGAGGTTTT GCAGTCTCCT CATTCGTTTA TCCCCTCCAC 780 GTTCTCAGCT GACTGCAAGA GGCTGCTCGT GTGAGCCACT CATCCTTCCA GCTGCAATGT 840 CCATCCCAAC GACATAATGG AGAGAGCATG GGCTTTAGGA GTTAGTCATG CTGGGGCACT 900 CATGCTTTCT CATGGCATGC ACTGGGGCAG CAACATGCTG TTTCTGAGTT TTAGCACAGT 960 GCCAGTGCTG AGAACAAGCC TCACGTCAGG CAGACCTGGG TGCGAATCCT GGCTTTGCCA 1020 TTTGCTAACC ATGAGGACCT GGGACATTTC TTTATTCATT TAACAAATGT GAAGTGTCTG 1080 CTATGTGCCA GCTACTCTAG TAGAAGCAAG GTCTGTGTTG GTGAAGATAA CCGATGTCTC 1140 CCTGTCTTTG CAGTTCTAGT GGGGAAGGCA GACAGCAAAC AAGGAAGCAG ATGTCTGAGT 1200 GGCCATGAGC AGGAGAGAGC CTACTCAGAC CAGGGCTCTA GGAGGGCTCT CTGCAGTGGA 1260 GCTGACACCC AGGCTGAGGC CTGAAAGATG GGAAGAAGCC AGCTGTGCAA AGAGGGGAGA 1320 ACACTCTGGG CTGAGGAATA GCACGTGTTC TGGGGATGGA AAGAAGAACA GAAATGAGGC 1380 TGTTATGTCA GGAGTGATGG GGTGGGATGG TGGCAGGGGT GTGTACTACA 1430
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