Tag | Content |
---|
EnhancerAtlas ID | HS092-28927 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:126737700-126739040 |
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 | CACAATGACA GTGCCTACTT TCCCTGGGTG CTGGGAGTCG TGGTGGGTTG GCTGGTGCCA 60 GCGGAGCAGC AGAGAGGGGT GCTTCCACCA TGCAGCAATG GGGAGCCCTT GCGCTTTGGC 120 AGTCCCTGGG CACATAGAGA TCTTGGCCTG AGCTGACCTT TGTCCTTGAG ATGTCTATAG 180 GGGGAGTCAT GCCACACCAT GCTCCTGATC AGGGCAGGTG TGAGTGGCAG AAATCTGTTC 240 CATGCCGGGC GAGACTTTGA GCGTTTGCAG ATAGTAACTC ACACATGTTC AGGGCTCTAG 300 GGGGCAGATA CTAGGAGTGT TCCTGCTGCA GTGTAGGACC TTAGCCATGT GGTCCAGCAT 360 GGGGTTGTCA TGAATTCCAC TGGGACTCAA CTGGGATGGG GTGTTTTGTT TGCACAGGAC 420 TCAGCCAGTC TTAAAATGCA AAGTTCTGCA TCCTGGGAGC CCTCTCAGTC CCAGACAAAC 480 CTAAGTGGCC CTGTGGTGGG CTGAGGGTCA CCCTACCTCT TGGGCAGCCC TGGTGGGACT 540 GGAGGCAGGT GTGTGTTGGG GCCAGGTGGG AGGCAGGTGG CCTGGACCTC CCTTGTGCTC 600 CCGCCTGCTG AGGCTGGCTG TCTGGCGAGG CTGGCGTGTG TGGATGCAGT GGCTGGTGGC 660 TGCTCCAGGC CAGCCAGGTG CAGATAACTA GACGCCTGGC AGCGATGCCC AGGAGACGAA 720 GACTCCAGCT CTTAATTAAA CCTGTCAGAT GTCCCCCAGA GCCTGCCTGG CACTCCTTTG 780 GCTTCTGATC AGATAGCCTG ATCCTCGGGC TGCCACAGGA CTGACACCTC ACAGCTCTGG 840 AATGTTCTGT CAGGGCCTGC CTGCCTTTGT TCCTGACAGA GGCAGAGCTG GCCCTGAGCA 900 GGGTGGGCCA TGTTGAGGGT GCACCAGGCC CGAGATGTGC ATGCAATGGT GTGGGGGCTT 960 GGGGACAGCC TGCAGCCCTG GGACCTCACC CCTGGCCGCA CTCCACCACC TCACAGCGGG 1020 TGGAAGGAGC CCGAACTCCA AAGCTGCTCT ACGCTTAACT GCCAGTGTCT GAGATGCAGG 1080 AGGCCCTGCC CAGCCTGCCC CTGGTGCTGA TGCTTTCTCT GCCCTTGTCT TGCTTGATCC 1140 TGTGGGAACC TTGCAGAGGA GAGTTACTAT CCCTGTGCTA GGGCTGTAGT AGCTGGGGGA 1200 CGAAGAGGCA CAGTAGTTTC CTTAAGATCA CGAAACCAGT AAGTGTCAGA GCCAGGATTT 1260 GATGTAGGCC CCAAGAGTGG GAGGGTTGGG GCATGGAGCG GGGCCACCAG GGCATGCTGC 1320 CCCTGACGCC GCATCTGGCC 1340
|