| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06761 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:120823670-120825400 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:120823702-120823721 | CACCGCCACCTCGTGTCCA | - | 6.09 | | EWSR1-FLI1 | MA0149.1 | chr11:120825380-120825398 | CCCTCCTCCCTCCCCTCC | - | 6.27 | | ZNF263 | MA0528.1 | chr11:120823761-120823782 | GGGGGAGGAGGAGTTGGGAAG | + | 6.07 | | ZNF263 | MA0528.1 | chr11:120823753-120823774 | GGAGGAGAGGGGGAGGAGGAG | + | 6.82 | | ZNF263 | MA0528.1 | chr11:120823747-120823768 | TGGGGAGGAGGAGAGGGGGAG | + | 6.97 | | ZNF263 | MA0528.1 | chr11:120823750-120823771 | GGAGGAGGAGAGGGGGAGGAG | + | 8.04 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I120952 | chr11 | 120823181 | 120824670 |
|
Enhancer Sequence | TCGGTACTCT CCTCTTCCCT TCCCTGTCCT TACACCGCCA CCTCGTGTCC ACCTCTGGGA 60
ACTGCATGGG GAGGGGGTGG GGAGGAGGAG AGGGGGAGGA GGAGTTGGGA AGATCTTGGT 120
GCCAAACTAG AAGGACAGGA GAAGGACTGG GGGCCTGAAA TGCTCTCTGC CCAGCTGTCG 180
ACCTCATGCT GCCCATCCAA ACATTCCCCA CTGTGCACGA CGCAGACAGG TGGCTTGGCT 240
TCTGCACCTC TGCCTCCTGT CCCCTCCCAC TTCTCCCCAG ACCCCCACCT AAGCCCCTTG 300
CTTGTGTAGG AGCCCTGGGA AGAGAGGAGG GGTGGGGTTG GCAGGAAGAT GACTCTCATT 360
AAGCACTGTG CATTTGGCTG CCCTGGCATC AGTCATTGCC ACAAAGGATC TGCCACAAAG 420
TGCCGAATGA CAAGGAACAG AGCCTGCAAA TCTGGACTGG GGGCACTGGG GGCTGCAGTG 480
GAGCAGGCCA GGGAGAAGGC TTTCTCTGCA GACAGCCTGG GCCTGCCTCT GAAAACACAG 540
CTGCCTTGTC GAATGGGAAC CATGGAGGCT GCTGGCGGGT GGCAAGGAGA CGGGATGGAG 600
AGAGGCGTTT TCAAGAAGTG CTGAGTTGAG ACGCACGGGC CAGACCAGGG AGGGGGGAGA 660
ATAAGCCCTG CCCTATCCCC AGGAAACCAG GGGCTGCCCT GGCCCTTTGG AAAAACCTGA 720
GGAGCAGCCT GAGGCTGTGG CCTCCCAAGA CTGTGCACAG CAAAGGTAGT TTCGCTCCAG 780
GCCAAGGCTG TTGGGCCAGC CTGAGCTGCA GGAGAGCCAG CTTAACCCTC CAGAAGTGGG 840
ATGAGCCCTG GTGGCTCCCA GGCCACTCAC TCAGGTCCCT AGTGCTGCTA ACCCTCCACT 900
TACTGCAGTG GAGGCTCACA AAGGGCTGTT ATGTGGGAGC AGAGAACTAC TCAGGAGGAG 960
CTTCTGGAAT CTGTCCGTGG CTCTGGTTTG CAGGTGTCTC TTCAGTTGTT ACCTTTGCCT 1020
CTAGGCCACA GTGGGAGGGC AGACAGTGTT AGAGTGCACA TCCCATCTCT GTGGGGTGGG 1080
TGGGGTCTTC CCCTAGGGCA CGTTCATTCA CTGGATTGAT GGGGGCACTT GGGGATGGAG 1140
CTGCCGCATG GTAAGCCCTA GGGAACCACG GGCTACCTAA CCCCTGAGGG CACTTCCCAG 1200
ACTGCCAGAG AAGGGTTGCA TCAACCTGTC TGCACATACC TCTTCTAGTG GAGACCAAGG 1260
TCCCCAAGAT CAGGAAGGTC TTTGGGGCCC ACAAGATGCA GCCAAAAAAA GACAGGCCTT 1320
GCTGACAACC TGGTCATTTT CAAACGTGGC AGAGTTTGCT GCTTGGGCAC CACCAACCCC 1380
TCTCGGGCCT GTAGGCATGG CCACTGTTGA GTATCTGCTG TCAGTGACGG CCTGCGAGAT 1440
GGGGAGCTAG CACGCTGTCT GACACCTCCC CTCTCCACTT TGCCACACTG CTGCCATGTT 1500
AGGAGGCTGT CTCCGTGAGC CTGGTGCCAC TGCTCTGTAA TTCACACTTG CCCCTTGGAT 1560
GTGAGCCCTT GCGTGTGGCA TGCCACAACA CTCAGGTCAC CTCAAGGGCC CTGAAAAGTC 1620
TTGGGGTTTG GAGAGCAGAT ACATACAAGC CTGCTTCAGC ATACCCACAG CAGCCTAGAG 1680
CTTTCAACCA GCCCTGGGGT GTTACGCTGC CCCTCCTCCC TCCCCTCCAC 1730
|
