Tag | Content |
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EnhancerAtlas ID | HS184-12514 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:67959750-67961170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr16:67960454-67960465 | GACAGCTGCTG | + | 6.14 | NR3C1 | MA0113.3 | chr16:67960532-67960549 | GGGGACAGAATGTACTA | + | 6.07 | NR3C2 | MA0727.1 | chr16:67960532-67960549 | GGGGACAGAATGTACTA | + | 6.16 | Tcf12 | MA0521.1 | chr16:67960454-67960465 | GACAGCTGCTG | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_03621 | chr16:67959303-67961429 | Brain_Angular_Gyrus | SE_41735 | chr16:67959309-67962864 | LNCaP | SE_47920 | chr16:67959415-67961789 | Pancreas | SE_65564 | chr16:67955732-67963378 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I067925 | chr16 | 67959742 | 67961132 |
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Enhancer Sequence | TCCCTGCCTC ATCCCTCTGT GGCAGTGGGG AAGGGGGTAG GGAAAGAGTT GGAGGTCAGG 60 CGAGCCAGAC TGGGAGTAGC AGTAGTCAGT GAGTGTGTGT GTCTGCTAGA TGGCTGTGCA 120 CCTGCCCTGA AGGTGGTCTC TCAGATCCTC CTGAACCCCC TGGAGGGCAT GTTCAGGGGT 180 TCCTCAAGGT GAAGGGTACC ATGGGTGGTG AAGGGTACCA TGGGTGGAAC AGGCAGACCT 240 CACCTGGCAG GAAGGAAAGT GAGGGGATCG TTAGCATCCC TGTTGAGTCA TCTGCAGCAG 300 GCTCAGGAAA GGTCCTAGCT GCCTATCCTT GGGGGAGCCT CAGAGCCCGT GCCAGAAGTG 360 TTCCTAGGAG ATGCAGGGAC GCAAGGACTC ACCTGGCTGA GCCCCAAGGC CTGGAAGCAG 420 CTCCAGGAAA GGGCACCCAT CCGGCAGCAC CGTGGGTTGT TTACTGTCTG AGCCTGTGCC 480 TACTGAGTGC TTCCTGTATG CGCAGCACCA GGCACGGGCT CATCCAGCTC AGCATGATCT 540 CATGGGAATA CTAAACGAAC ATGAAATTGC AGTCTCACGT TACAGCTGGA ATAATTGCTG 600 GAAGCACTGG GGGCTAAGAG GGAGTCTGAG CAAGTGTCCT TTACCCTGAG AACCTGAGGA 660 TCCAGTCAGG TGAAGACAGC CGTACAACCT GAGGCCCTGA GACAGACAGC TGCTGGGTTC 720 GGGGCTGAGA TGAGGCAGCC CGGGGTGCAT GTGGCAGAGT GGGCTTTATG GAGTTCCTCC 780 CAGGGGACAG AATGTACTAA AATGAGGCTG GCGCACAGCA CTGCCAGGAG CCCTTTGTGG 840 CTTAGAGAAG TAATGCGGGC CAGAGGGTGC CACTGAGAAG GGTCCTGGTT CCTTCCTGGT 900 CCCGGGATCG CCTGCCCTCA GCCGACTGGG AAATCTAGTT GCCTTGAATT GTTTCCTTTC 960 CTCCCCATGC CGGGAGGCAG AGGCAGGGAG CAGTGGTCTT CTGCCACTGC TTCGGCAGTT 1020 GGAGAGAGGT TGGATCTTCT CTGTAAGGAC TAGGAAGTTC CCCTTTAAGT AGCCTGATCC 1080 TGGTCATCCA GAGATTGGAG CTTCAATCTG ACTTAGGATG TGGTGGGAAA GTTTGAATCA 1140 TTCTCTAACA GTCCCCTGAG TTATGATACT CCTGGGACAA GTTCGGGGGG GTCTTGGCAG 1200 AGGCCATCTC CCTGAGCCAG GCTTTGGGTC CAGTGCACCA TAGAATTTGC TCCCTGGGAG 1260 AGTGCACAGG TCCTTTCCTT CCTTGCCAGA CTCCATCACC TGGAGAGCAG CCCTTGTTCA 1320 GCCTGAGCCA GCGTTGGGCG GGGAGGCCCC AAGTGCTACA TGAGAGGAGG GGCAGCACCT 1380 CTCTCTGGAA AGGGGAGGGT TGCTGAGTAG TGGCCTCATC 1420
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