| Tag | Content |
|---|
EnhancerAtlas ID | HS105-85616 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chrX:152804600-152805960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:152805116-152805135 | TGTCCACCAGGTGTCAGTG | + | 6.49 | | Myog | MA0500.1 | chrX:152804811-152804822 | GACAGCTGCGG | + | 6.32 |
|
| | 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 |
| GH0XI153537 | chrX | 152802498 | 152805170 |
|
Enhancer Sequence | CACCTGGCTT AGCTCCTGTA ATTCCAGGAG ACAGTCCCAG TCCAGAGCGA GGTGCACACC 60
CCTCAGTTGG GTCCCTGGTC CCCAGCCCCC TCCCCACCAC CCAGGAGCTG AGGTCGTGCG 120
TTAACCCCAG GCTCCCGATT GGGGCAGGCT CGGGCCTCAG CAAGAGGCCT TTGGCTCCTG 180
AAGAAACCTG AGCCAGGGGC AGAGAGGCAC GGACAGCTGC GGCTCTTCTG GGTGGGGAGG 240
ACGCCATGTG GCCGTCGCCT AGCTGGGGTG AATGAGCCAC GGTTGTGCGG GCGGCAGCTT 300
CTGTTCCACT GCGGCCAGGG CTACCCCTGC CCCTCCTCAG AAGCCCCAAG GTTAGCATGC 360
GCCTGTTCTC CAGTCATCTG GAGGGTCTTG TGTGCCTTCC CAGACCCACT GTGAGTGCCC 420
CATGGGCTGG GGCTGGGCTC TCTGGTCATC CCGTCCCTGC AGCAGATGGC AGGCGTGAGC 480
CCAGCTGCCC AGGGCTGGGA GCTGCAAGCT GCTGTCTGTC CACCAGGTGT CAGTGTGGGT 540
CTGGTCACGG CCGCGACAGC ACTGGGCGCC GGGTGAGCGC CCGGGAGGGC TCCTCGGGAT 600
CAGCCGGGGC TGAGAATCCT GGGGCCAAGG GTGGGGCCAG AGGAGGGTGT CATCCCACAT 660
GCCTGCCCCG GTAGAAGGTG GCTGAGTGGG TGTCCAGGCC CGGATGCCAG TCACGCACGT 720
AAGCTTCCAG TACCTTCAGG CCAAGGAAGA CTGAGAAGTA AGCGTCCTCA AGGATGACAA 780
GTGACAGAAT TGGATAGGGA CAGGTGGCTC TGATTGTGAA GGCAAAGCCA ATTTGGGGGC 840
TTCTGAGTGG CTTTGGGTGT CATTCAAGTC GCCATGTAGA CAAGCTGTGA GCCCTGGCTG 900
AGGGATCAAA GTTGGTGCTG GAGTTGCATT AGAACCAAGG CTGCTGGGTC CTGAGGGCCC 960
TGTGCTCACC GGGTCCTGTC GGGCAGCGTA GGTTCTGTCC TGACCTGGGC CACAGGCCAG 1020
AGCTCTGACT CATGGTTACA GGGCCCTCTC CACCTCCGGC CTCAGTGGCC TTGTCTGCAC 1080
CCTGCAGAGA GCAGCTGATG AGCAGCCCAG GGTGGGCAGT GTCTCCCCGA CCCCTGCGAG 1140
GCCATGCAGC CCAGAAAAGG CTTGAAGACT TCCCAGTCCC CTCCCTCAGC ACCGTGACTC 1200
CGGTTTGGCT TCTCCCCGCC TGTTCCCCAC CAGGAACCCA CTCCCATTCC CGTGCCTCTC 1260
TCTCTCCTCG CGTGACACCG TTCTTCTTCT TTGGGTCTCT GGACCCAAGA ACTTGCATCT 1320
CCCATTAGCT CTCATGCTCC CTCCCCACTG CTTCTTCCCC 1360
|
