| Tag | Content |
|---|
EnhancerAtlas ID | HS129-11862 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:71184780-71186050 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:71185190-71185208 | GGAAGGACTGGAGGCAGG | + | 6.09 | | EWSR1-FLI1 | MA0149.1 | chr14:71185870-71185888 | GGAGGGAAGGGACGAAGA | + | 6.09 | | EWSR1-FLI1 | MA0149.1 | chr14:71185874-71185892 | GGAAGGGACGAAGAAAGG | + | 6.64 | | KLF4 | MA0039.3 | chr14:71185642-71185653 | ACAGGGTGTGG | - | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr14:71184955-71184970 | TGAACTCCTGACCTC | - | 6.22 | | TEAD1 | MA0090.2 | chr14:71185622-71185632 | CACATTCCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27225 | chr14:71183631-71184911 | Esophagus | | SE_27225 | chr14:71184919-71186254 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I070716 | chr14 | 71183599 | 71186039 |
|
Enhancer Sequence | GTGCCATCTC GGCTCACTGC AACCTCTGCC TCCCGGGTTT GAGCAATTCT TCTGCCTCAG 60
CCTCCAGAGT AGCTGGGACT ACAGGCACAT GCCACCACAC CCAGCTATTT TTTTTTTTTT 120
TTTTTTTGGT ATTTTTAGTA GAGACAGGGT TTCACCACGT TTGCCAGGCT GTTCTTGAAC 180
TCCTGACCTC AGGTGATCCA CCTGCCTCTG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA 240
GCCACGGCAC CCATGGTGAC CACTTACAGG TTGCAGTCTT CTTAAGACAC CTAGGTAGAT 300
AGCCAGAAAG TCAGTTCATA AAGAGGATAA TACTCTTTCA AGCAGGAGGC CTCCATTCCT 360
GGAAAATCAA GTGTTTCAGG AAGCAGAGAA GTGTTGAGTC TTAGGGATGG GGAAGGACTG 420
GAGGCAGGGA AATTGTGATG GGCATTTGGG AAGGTAGACT CAGGTCAGAT TGGGTGGGGC 480
CCTGAAGGCC GTGCTCAAGA ATGTGGATCC TTTCCTGCAG ACATTGGGCG TGGCGTGATC 540
CAACCTGTGT TCCATGAGCA CATTTCCTAG GCTGATCTTT CTCAAGCCTC CCCATTGTCC 600
TTACGTCACA AAGAAGTGTC CAGTGCCTCC CACTGAGACC CCATAACAGG CACTCCTGGT 660
TGGATAGCAG CAGTGTGACC AATGACTGAG AGGAGGAGGG GACAGAGTGG CAGACCCCCA 720
CCCTCATCTC CACCCCACCC CCTTATGCCA AAACATGTTC TCCAGCTTGA GCTAGTTGGA 780
CTAGATCGGG TGGGGACCAA GGGCTCAGAG GATTAGGACA TCAGCCCCAG CCTTGAATGA 840
ACCACATTCC ATAGGCACGT AAACAGGGTG TGGTGGACGC AGGCCTGGTG CAGCTCCTTT 900
GACAGAGGGG TGTGCACTTG TGTTGTAGGA ACGTGCTATT TGCCTGTGCA GGACCTGACA 960
TCCCTAACCA GCTGTGCCCC TAGGAAACCC CCACAGCACC TCCTTCTTAG AATGTTCTCT 1020
GTACATGTGC CCTCACTGGA TTCTGCTAGC AGTCTGCAGG TGCTCACCAT TCCAGCACCA 1080
ACTCTCCACT GGAGGGAAGG GACGAAGAAA GGGGTGAGGG GGACCAGGAA GTTGGCCCCA 1140
GTCCTACCTT CCATAAGCAG GGCTTCTGGA ATCACCTCGT TATACTGCTT AGGGCAGGGG 1200
ACAACCTTGA AGCCAGTGGC CTCTGGAACA CCTGCAAAGG AACCTGGTTA GCATGGGAAA 1260
GCATCCTCAA 1270
|
