| Tag | Content |
|---|
EnhancerAtlas ID | HS052-10052 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:132344960-132346020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:132345034-132345052 | GAAAAGAAGGAAAGAAAG | + | 6.23 | | EWSR1-FLI1 | MA0149.1 | chr12:132345043-132345061 | GAAAGAAAGGAAAGAAAG | + | 6.33 | | IRF1 | MA0050.2 | chr12:132345019-132345040 | AAAGAGAAAACAAAAGAAAAG | - | 6.12 | | IRF1 | MA0050.2 | chr12:132345013-132345034 | GAAAAGAAAGAGAAAACAAAA | - | 6.45 | | ZNF263 | MA0528.1 | chr12:132345342-132345363 | GAGGGAAGAGGGAGGGAGGGA | + | 6.45 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_43473 | chr12:132344856-132347817 | MCF-7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I131859 | chr12 | 132344299 | 132349032 |
|
Enhancer Sequence | CACTCATTTA AAAAGAAAGA AAAGAAAGAG AGAGAGAAAG AAAAGAAAGA GAAGAAAAGA 60
AAGAGAAAAC AAAAGAAAAG AAGGAAAGAA AGGAAAGAAA GATCAAAACT AATCCAATCG 120
GTCTCAGCCA AGCTAGGTCC TGGGGCCACA GGAGGATCCC TGCAGCCTGT TGCATGAATC 180
AATCAACCTT CCCTGGAACA CAGCCAGGCC CATTTGTTTA AATAATAATG CACTAAACAA 240
GGCAGCGGAG CGGTGGGCTG GCCTCTGGGA GAGGTGACAC AGCAGCTTTT AGTTGTCACA 300
ACACTCGTTT CCCAAGCACA AAGAGAAACC AAAGGACGCG CAGAGGAAAG GTGGTCTCCC 360
GGCTGGGGAG GACCTGGGAT GTGAGGGAAG AGGGAGGGAG GGAGCAGGGA TGCATGAGCC 420
CGGCTCTGGG GCTCCTGCAC CCCTCAAGGC AGGCTGAGGC CGGCCTCGCC CTGGTTGCAT 480
CACCCAGGAC GCCCTGGGGA TCTCCAGGCC ACCGTGGCAG CCGGGCCCCT GATGCAATCC 540
ACGGCTGTCT GGCAGCATGA CCTGCCCCGG TCAGCCTGGA CTCTGCCCTG CCTGGGGGCC 600
CAGCCCTGAC CACAGCCTCC AGCGATCCCT CCCTTCCCAG GGTCTGTTTA CAGGCGCTTG 660
GAGCATCAGG CGCATTTCTA TCATGAACTC ACAGGGTGGT GCCCAGCGAG TGTCTCTGAT 720
CTGTAAACTG GGTGTGGTGG CATCTACCCT GTCTGTGGGG TTGCAGGAGG AAGCCACACG 780
CATGTGGGGA GCCATGCCAG GCACACAGTG GATGCAACAG GGGAGTTGCT CGTTCTGACC 840
GTGTTCACCA TGTCTCTGAT GCGCATCTTC TCACGTGAAA TCAGCATGTG TCTTAAAATG 900
GACAGAGTAG AAGTTCAACT AGCAACATTG TGTGCTTCCT ACTGGCACAT ACGTGAATGG 960
TGGAGGCTCA CGCCTCTCAA CCCAGCACTT TGGGAGGCCC AGGCTGGAGG ATCACTTGAG 1020
CCCAGGAGTT CAAGACCAGC CTGGGCAACA TGGTGAGACC 1060
|
