| Tag | Content |
|---|
EnhancerAtlas ID | HS183-13748 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:130986660-130988310 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:130987475-130987493 | CCCTCCAGCCTCCCTTCC | - | 6.28 | | EWSR1-FLI1 | MA0149.1 | chr9:130987479-130987497 | CCAGCCTCCCTTCCTTTC | - | 6.35 | | ZNF263 | MA0528.1 | chr9:130988282-130988303 | CCTCCTGTCCCCACCTCCTCC | - | 6.3 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAAGAAGGT AACCCGGAGG CCCGGGCCAG CCCCCACCGC CTCTGCCCCG CCCTGCACTG 60
CTGCCAGGCG CTCCTTCCCC ATGTCCCCCC CTGCCTCCTC GGTAGCATGT ACAGACCTCA 120
GCGGGGTGGG GAGGCAGGCC ACCACTGAAT AGGAGACAAT GTGCCTCTGA GAGGGCCTCA 180
CCCACCCCTG GCCCCCAGGT CTGGGGACCC AGGGATTGGA CATGGGTGAG ACGGGGATGA 240
TGGCTGGCTG TTTACCCCAA GAGCCCACCA AGAGCTCCCC CAGCTCAGAG AATAGGGCTT 300
GAGGGGACCC TGAGCCCCCT CCCTGTCCTC GGAGGTGTCA TCTTTGGGAG CTCCAGGGAG 360
GGGTCTGGGG AAACCTTAGC CTTGGAGACA GGTGAAATGC AGGGCCTTCT CGGGCACTGC 420
TCGGTGGGCC TGGGTGGCCA GAGGGGGTGC AGAGGACCCA GGACTAGCAG GTGCCCTGGC 480
TCCCCGCTGT CCTTCATCCT CCCCATACTC ATCTCACCCT CACTCAGGAC CCTCACACAG 540
GATGCTCACG TAAGACCCTC ACTCAGGGCC TCTCCCTCCC TTCCATCCAC ATCTGGCTTT 600
CCAGGGATAG AGCCCTTCTC CCATCTGCCC CACCATCCAA GCCTCACAGA AGCACGCAGG 660
GAGGCAGGAC AGGGAGGACG GTGCCCATTT CACAGCACGA ACACTGAAGC TCCAGGAGAT 720
CAAGTGGCTT GCCCAAGTCA CAGTAGTCAG GAGGTGGCAG AGCTGTTACT TGAAGCCACG 780
GCTCTGGACT CCAAGTCCAG TGCTCCTCGA TTCCACCCTC CAGCCTCCCT TCCTTTCCTC 840
TCCCCACTGC TGTCCCGGCC CCTCTCTATC ACTACCTCTA CTCTTTCTGT CTTTCCTCTT 900
CTCTTTCTGT CTTTTGGTTC CACCAAACCC CTGTGGAGGA GAGGCCAGGA ATGCCCCTTG 960
AAGAGAAAGG GAGGGGCGGG ACTAGAGCAG GGAGCTGGAG AGGGAGGTCA GGCTGCTATA 1020
CTGCAACCCT AGGAGGCAGC CTCTGCGCCA CGGTTTACGG GAATGGACCC CCCTGGAGTT 1080
GTGCAGTGCA TGGCCTGGGC AGCTGGATGC GGCAACCCTA GAGATAGGGA ATGGTACTGA 1140
GGTTTGGAGT CAGGATGAAG CAAATTCTGG GACACTGGGA AACGTAGAAT TGAACAGGAT 1200
GGGTGGATGA GGTCCTGGCC TTGTCCTGGC CTGGGTCAGC TCCTTAGGAG AACCCAAGGC 1260
TGTGGACAAA GACGGCACTG GGAGAGAGCA GGCAGCCTCA GTGAGGCCGA GGAGCAGGGG 1320
AGCATCCCTG GGAAGAGGAT CTGAACTCAA TAGGGGTCTT GTACGGAGCA GGGGCTTGGT 1380
CCCTCGTACC TCTGGCCATA CCTATGGAGC CCAGGGGATG CTTGGCAGCA CCTGGGAGGT 1440
GCCAACCCCG GGTGGCAAGG GAGGGCCGGT CCCACGCTCA CATTGTCTTC TGTTCTCTCT 1500
CTCTCTTTAT CTGTGTCGAT GTCTCTCTCT CTTCCCCCGT GCCCGTGCCA TCCTCTCCAC 1560
CCCTGGATTC CTGTCTCTGC TTGGCTTTCA CCCACTTCTC CTCCCCACCC ACGGCTGCTC 1620
CTCCTCCTGT CCCCACCTCC TCCCCGGGTG 1650
|
| |
|
|
|
