| Tag | Content |
|---|
EnhancerAtlas ID | HS098-24770 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:61570140-61570790 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR3C1 | MA0113.3 | chr17:61570477-61570494 | AAGTACACAATGTCCCA | - | 6.21 | | NR3C1 | MA0113.3 | chr17:61570477-61570494 | AAGTACACAATGTCCCA | + | 6.75 | | NR3C2 | MA0727.1 | chr17:61570477-61570494 | AAGTACACAATGTCCCA | - | 6.23 | | NR3C2 | MA0727.1 | chr17:61570477-61570494 | AAGTACACAATGTCCCA | + | 6.49 | | SCRT1 | MA0743.1 | chr17:61570527-61570542 | AAGCAACAGGTGGTG | + | 7.02 | | SCRT2 | MA0744.1 | chr17:61570527-61570540 | AAGCAACAGGTGG | + | 7.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGAAGCCGA GGCAGGAGGT CTGCTTGAGC TCAGGGGTTC GAGACCATCC TGGGCAACAT 60
AGCGAGACCC CATTTCATAA AAAATAAATA AGTAAATGAG AACAAGGAAG GACTGACGAG 120
AGACGGTAGA ACCTTCTGGT TTGGGCAGCT CTGCAGCTGC CATTCATCCT GGCCATAAGA 180
ATTCTTGGGG TGAATAAGTT TGTCGCTGTT GGGCCGCATG AGATGCAGAA TCGCCCACTC 240
TCACCCCTGA CAGAAACAGT TGTTTCCTTC AGGGAGCCTC CATCTTGGGA GATAAAGCAT 300
GTGTACATGG GAACCCACTG GCCACACATT CTCTAGAAAG TACACAATGT CCCAGTGCCT 360
CTAGAGCAAG CACTTTGTAC AGTCAGAAAG CAACAGGTGG TGGGGGCTGG AGTCATTCAG 420
GAAAATGGGA GGCAGAGGAA TGGCCTGAAC GGCCCGATGC TAGGGGCTTC TGCCCCCAGA 480
TTCCCTCTTA CGCACACTCA GTGGTTGCCC TTCCCCTCCC TCCCCACAGT GCTGTGTCCC 540
CTGCATGCTG CAGTGCTGGG GTCTGCCCTG GGTATAGCAA GGCCCACTGT TCCCTTATGC 600
CCAGGGCTTC TCACTGTCCT CTCCCAACAC CCTCTCCCCC ACTCCACTAT 650
|
