Tag | Content |
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EnhancerAtlas ID | HS183-01336 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr12:116974320-116975810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr12:116975707-116975719 | CAGCACGTGGCC | - | 6.37 | REL | MA0101.1 | chr12:116975296-116975306 | GGAAATCCCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09669 | chr12:116974878-116978431 | CD14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I116536 | chr12 | 116974376 | 116978655 |
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Enhancer Sequence | CCATGTTGCT TTGTGATCTC TGCCTCTCTC TAGACCATTT GGCTCCTATG CACAGGCAGC 60 TATGTCTTTT TCATATTTGG GTCCCCAAAA TGCACAGTGC GGTGCCTGCC TCAAAACAAA 120 TGCTTTTCAA TCCGTCAATC AATCAGTTGA CATGGATCAT CTTTTCTCAG CACTGATGTA 180 TGGACTACAA CTTGGAATTC CATTAAAGCT CCTGGGGTCA AGAAAAAAAG TGATTCAAGT 240 TTATTTATTT ATTTTTTTTT GAGACAGAGT CTCATTCTGT CGCCCAGGCT GGAGTGCAGT 300 GGCACGATCT TGGCTCACTG CAACCTCTGC CTCTGGGGTT CAAGTGATTC TCACTCATGC 360 CTCAGCCTCC CAAGTAGCTG GGCAAGAGCC AGCACACCCG GGCTAATTTT TGTATTTTTA 420 GTAGGGACGG GCTTTCGCCA TGTTGGCCAG ACTGGTCTCG AACTCCTGGC TTCAAGTGAT 480 CTGCCCACTT CAGCCTCCCA AAGTGCTGGG ATTACAGGCA TTTAATCACT GCACCCGGGT 540 GAGCCACTGC ACCCGGCCAA GTTCATATTC TAAAAGTGAA ACATTAATGC TGCATTGTGT 600 ATTTTTTGGT CAAGTGCTTC AGATGTGTGG AAGGAATTTC TTTGTATAAA TGCAATTATT 660 CGTCACCATG ATGATAATTA TAACGAGGGT GACTGCACAG AACTGTGCCT CCCCAGCAAG 720 CATGGGCTGG GCAGGGCCGG GTATTCCCTT CGCTGACTTG CTTCACTAGT TGACTAACAG 780 ACCTTATTCC CGGGCCTGAG CTGATGATAT CCTGCCAATG CCAGCTTCCC AACATGGAGG 840 GGACGCAAGA GCGAGCGCCA TGGGATCCTG GGGGAAAAGC AGCCTGTGTT TGCTGCTGCT 900 TTGACAGTTG AGGCTCTGAG AGGGACTGGC AAACAATGGG AAATGAAACA TTTGAGTGGT 960 TGCAAAAAAT TCCATGGGAA ATCCCCCCTG GTGGTATTTA TGTGCGACGG CTGTGACAAG 1020 GAGAGCGCAG GGCTTTCGAT TTCAAGGGTT CCTGAGCAGA CCACAATGGC CTTCCAAGAT 1080 GGCAATCCCC GGGAACAGCT CTCTCGGCCA CAAAAGGCCA GTTTGTCTGT CCAGGGAAGA 1140 TCTGGCCCCA TGCATCAAGT TGGCCATGAG CTGCAGTGTC TTCTTTGGGG CATGACCCAC 1200 ATTTATAGGG TCTGGGCCTC TGAACCTTCT GCTCCTAAGA CAGATCTATC TCAGTTGTCC 1260 CTCTGGTTTT CCCAGGCCTC AAGGACCTGG GGGCTGATAG GGGCTGAGGG GTTTCCCTCG 1320 GGCTCAGCCT CCATCTGCAG AACTGTGGGA ACCTCAGCCT CCATCAGACC CCTCCCCATT 1380 TTCTGGTCAG CACGTGGCCT CCTCCTGTTT CCTCCATTCC CGTTGGTAAT GGACATTTAT 1440 TTAACTTTTA CTCCCCCTCC ATTCTCATTT AGAAAAGAAA GTGAACTGAT 1490
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