| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20874 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:126737370-126739040 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:126738555-126738573 | CCTGCCTGCCTTTGTTCC | - | 6.36 | | HNF4G | MA0484.1 | chr3:126737853-126737868 | TGACCTTTGTCCTTG | - | 6.02 | | Nr2f6 | MA0677.1 | chr3:126737853-126737867 | TGACCTTTGTCCTT | - | 6.31 | | RREB1 | MA0073.1 | chr3:126738091-126738111 | TGGGATGGGGTGTTTTGTTT | - | 6.06 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01881 | chr3:126736408-126740601 | Aorta |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I127019 | chr3 | 126738421 | 126738570 |
|
Enhancer Sequence | GGTCTGTTGG GGCCAGGGCT CACTGGGGCA ACTGCCACCT CCGAGCCAGG CCCTGGCCTG 60
TCCCCACACC TACTTCCCAC CGCCGCCCCC ACCCTGCTTC AGCTCAGTTT ACAATGTTCC 120
TGATAGCCTT GCTGTGCCAG AGCTGGTCCC AGGGCAGTGG GCGGGTGCCT GACCAGGGCC 180
TGGCCCTGCA GCAGGTACCA CCTCCTTGGG GTGCTGCTTG CGACACAGAA CCCAAAGCCA 240
GACTGTTTGC ATTTGTATCC CAGCTGGGCT ATAAGGCTGA AGGTGGCTAC TTACCCTTCT 300
GTGGCTCAGT CTTGTCGTCT CTAGAGTGGG CACAATGACA GTGCCTACTT TCCCTGGGTG 360
CTGGGAGTCG TGGTGGGTTG GCTGGTGCCA GCGGAGCAGC AGAGAGGGGT GCTTCCACCA 420
TGCAGCAATG GGGAGCCCTT GCGCTTTGGC AGTCCCTGGG CACATAGAGA TCTTGGCCTG 480
AGCTGACCTT TGTCCTTGAG ATGTCTATAG GGGGAGTCAT GCCACACCAT GCTCCTGATC 540
AGGGCAGGTG TGAGTGGCAG AAATCTGTTC CATGCCGGGC GAGACTTTGA GCGTTTGCAG 600
ATAGTAACTC ACACATGTTC AGGGCTCTAG GGGGCAGATA CTAGGAGTGT TCCTGCTGCA 660
GTGTAGGACC TTAGCCATGT GGTCCAGCAT GGGGTTGTCA TGAATTCCAC TGGGACTCAA 720
CTGGGATGGG GTGTTTTGTT TGCACAGGAC TCAGCCAGTC TTAAAATGCA AAGTTCTGCA 780
TCCTGGGAGC CCTCTCAGTC CCAGACAAAC CTAAGTGGCC CTGTGGTGGG CTGAGGGTCA 840
CCCTACCTCT TGGGCAGCCC TGGTGGGACT GGAGGCAGGT GTGTGTTGGG GCCAGGTGGG 900
AGGCAGGTGG CCTGGACCTC CCTTGTGCTC CCGCCTGCTG AGGCTGGCTG TCTGGCGAGG 960
CTGGCGTGTG TGGATGCAGT GGCTGGTGGC TGCTCCAGGC CAGCCAGGTG CAGATAACTA 1020
GACGCCTGGC AGCGATGCCC AGGAGACGAA GACTCCAGCT CTTAATTAAA CCTGTCAGAT 1080
GTCCCCCAGA GCCTGCCTGG CACTCCTTTG GCTTCTGATC AGATAGCCTG ATCCTCGGGC 1140
TGCCACAGGA CTGACACCTC ACAGCTCTGG AATGTTCTGT CAGGGCCTGC CTGCCTTTGT 1200
TCCTGACAGA GGCAGAGCTG GCCCTGAGCA GGGTGGGCCA TGTTGAGGGT GCACCAGGCC 1260
CGAGATGTGC ATGCAATGGT GTGGGGGCTT GGGGACAGCC TGCAGCCCTG GGACCTCACC 1320
CCTGGCCGCA CTCCACCACC TCACAGCGGG TGGAAGGAGC CCGAACTCCA AAGCTGCTCT 1380
ACGCTTAACT GCCAGTGTCT GAGATGCAGG AGGCCCTGCC CAGCCTGCCC CTGGTGCTGA 1440
TGCTTTCTCT GCCCTTGTCT TGCTTGATCC TGTGGGAACC TTGCAGAGGA GAGTTACTAT 1500
CCCTGTGCTA GGGCTGTAGT AGCTGGGGGA CGAAGAGGCA CAGTAGTTTC CTTAAGATCA 1560
CGAAACCAGT AAGTGTCAGA GCCAGGATTT GATGTAGGCC CCAAGAGTGG GAGGGTTGGG 1620
GCATGGAGCG GGGCCACCAG GGCATGCTGC CCCTGACGCC GCATCTGGCC 1670
|
