Tag | Content |
---|
EnhancerAtlas ID | HS184-13419 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:37159290-37159900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:37159426-37159444 | TCTTCCTCCCATCCCTCC | - | 6.12 | EWSR1-FLI1 | MA0149.1 | chr17:37159462-37159480 | CCTTCCTTTCTTCCCCCC | - | 6.73 | EWSR1-FLI1 | MA0149.1 | chr17:37159458-37159476 | CAGTCCTTCCTTTCTTCC | - | 7.21 | HNF4G | MA0484.1 | chr17:37159787-37159802 | TGCCCTTTGGCCTCT | - | 6.13 | ZNF263 | MA0528.1 | chr17:37159294-37159315 | TTCATTTCCCCCTCCTTCTCC | - | 6.17 | ZNF263 | MA0528.1 | chr17:37159429-37159450 | TCCTCCCATCCCTCCTCCCCC | - | 7.27 | ZNF263 | MA0528.1 | chr17:37159426-37159447 | TCTTCCTCCCATCCCTCCTCC | - | 8.95 |
|
| 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 |
GH17I039001 | chr17 | 37157764 | 37160084 |
|
Enhancer Sequence | TCTGTTCATT TCCCCCTCCT TCTCCGGGGC CTTCTCCGCT CCACCAAATG CCCTCTGCCT 60 CCTTCCTTTC CCATCTGGCT GTTTTCTTCT TTTCCACCTA CAAATCCATT CTCAGCTCAC 120 CCATTCTAAA AACAAGTCTT CCTCCCATCC CTCCTCCCCC TCGAGCCACA GTCCTTCCTT 180 TCTTCCCCCC ATTGCTGCCA AAGCCCTTCA AAGAGTGTTT TACTGGCGGC TTCCGGATCT 240 CACCACCCAC TTCTTTCTTA ATCGGCACAA TCTGGATCCG CCCTCAGCAC GTCACAGTCC 300 GTGGATCCTC TGAGAACTCC TGTGACCTCC TATTGCTGCT GGATTGCAGG CTCTTCTCGG 360 GCTTGATCTT GGAAGCATCT GGCCCTGCTG AAACCCTCCT CCTTGGCGAT AGGGATCCTG 420 AACTTTCCCC ATTTTCCTTT TCTCTCTCCA ACAGTTGCTT GTTCTCTTCC CGTAAGTGTT 480 GGCATCCTCG AGACTCTTGC CCTTTGGCCT CTTGTTTTCT CTCCTTCCTG CTTCGTGATC 540 TCACCCACTC CCAGGACTGC CATCAGGCCC TCTTTGCAGA TGTCTTCCCA GACTGCCGTT 600 TAGCACTGAG 610
|