| Tag | Content |
|---|
EnhancerAtlas ID | HS108-43061 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chrX:152804680-152806110 |
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 | CCCAGCCCCC TCCCCACCAC CCAGGAGCTG AGGTCGTGCG TTAACCCCAG GCTCCCGATT 60
GGGGCAGGCT CGGGCCTCAG CAAGAGGCCT TTGGCTCCTG AAGAAACCTG AGCCAGGGGC 120
AGAGAGGCAC GGACAGCTGC GGCTCTTCTG GGTGGGGAGG ACGCCATGTG GCCGTCGCCT 180
AGCTGGGGTG AATGAGCCAC GGTTGTGCGG GCGGCAGCTT CTGTTCCACT GCGGCCAGGG 240
CTACCCCTGC CCCTCCTCAG AAGCCCCAAG GTTAGCATGC GCCTGTTCTC CAGTCATCTG 300
GAGGGTCTTG TGTGCCTTCC CAGACCCACT GTGAGTGCCC CATGGGCTGG GGCTGGGCTC 360
TCTGGTCATC CCGTCCCTGC AGCAGATGGC AGGCGTGAGC CCAGCTGCCC AGGGCTGGGA 420
GCTGCAAGCT GCTGTCTGTC CACCAGGTGT CAGTGTGGGT CTGGTCACGG CCGCGACAGC 480
ACTGGGCGCC GGGTGAGCGC CCGGGAGGGC TCCTCGGGAT CAGCCGGGGC TGAGAATCCT 540
GGGGCCAAGG GTGGGGCCAG AGGAGGGTGT CATCCCACAT GCCTGCCCCG GTAGAAGGTG 600
GCTGAGTGGG TGTCCAGGCC CGGATGCCAG TCACGCACGT AAGCTTCCAG TACCTTCAGG 660
CCAAGGAAGA CTGAGAAGTA AGCGTCCTCA AGGATGACAA GTGACAGAAT TGGATAGGGA 720
CAGGTGGCTC TGATTGTGAA GGCAAAGCCA ATTTGGGGGC TTCTGAGTGG CTTTGGGTGT 780
CATTCAAGTC GCCATGTAGA CAAGCTGTGA GCCCTGGCTG AGGGATCAAA GTTGGTGCTG 840
GAGTTGCATT AGAACCAAGG CTGCTGGGTC CTGAGGGCCC TGTGCTCACC GGGTCCTGTC 900
GGGCAGCGTA GGTTCTGTCC TGACCTGGGC CACAGGCCAG AGCTCTGACT CATGGTTACA 960
GGGCCCTCTC CACCTCCGGC CTCAGTGGCC TTGTCTGCAC CCTGCAGAGA GCAGCTGATG 1020
AGCAGCCCAG GGTGGGCAGT GTCTCCCCGA CCCCTGCGAG GCCATGCAGC CCAGAAAAGG 1080
CTTGAAGACT TCCCAGTCCC CTCCCTCAGC ACCGTGACTC CGGTTTGGCT TCTCCCCGCC 1140
TGTTCCCCAC CAGGAACCCA CTCCCATTCC CGTGCCTCTC TCTCTCCTCG CGTGACACCG 1200
TTCTTCTTCT TTGGGTCTCT GGACCCAAGA ACTTGCATCT CCCATTAGCT CTCATGCTCC 1260
CTCCCCACTG CTTCTTCCCC GAGAAACTTC TGGAAAGTAA GCCTCCGCTC CCTGTTGCCA 1320
GCAGCCACAG GCACCCTGGA GACTGCTGAT TCCTCGGCAC TGGCCGTGCT CATGCCCCAA 1380
TCCCTCGGGC CCTGCCCACC CTCTTTGCAG GCTGTCCCTG CCCCCACAGG 1430
|
