| Tag | Content |
|---|
EnhancerAtlas ID | HS108-10452 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:111219220-111220330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:111219655-111219673 | GGGAGGAAGGAAGCATGG | + | 7.09 | | IRF1 | MA0050.2 | chr12:111219363-111219384 | AAAAGAAAAGAAAAAGTAAAG | - | 6.45 |
|
| | 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 |
| GH12I110781 | chr12 | 111219532 | 111219716 |
|
Enhancer Sequence | GCAGGCGCCT GTAATCTCAG CTACTCAGGG GCTGAGGCAG GAGAATTGCT TGAACCAAGG 60
AGGCAGAGGT TACAGTGAGC CGAGATCTCA CCATTGCACT CCAGCCTGGG CGAAAGAGCC 120
AGACTCTGTC TCAAAAAAAA AAAAAAAGAA AAGAAAAAGT AAAGTTCAAA ACCAAGTTAT 180
TCCAATAGCC TGGCCATGGG ATCTTCCTCT AGGTCCCAGA AGCCCAGCCC CTGGGATTTC 240
TCTGACAGCC TGTGCACAGG CTAAAGGAGC TGAAGTCTTC CCTGGGCCAT CCTTGCCACC 300
CACAATCCTG AGTGGTGACT GGATGTGCAG GGCAAGGCAT GGTGACGGGA CCTGCGGGGG 360
CCTGCAATGG GGACTTCTCT AGGCGATTTT ACTCAGGATT TCCAGGCAGT TCTAAATTAC 420
ACTATCCCAG TAGCGGGGAG GAAGGAAGCA TGGTTATCTG GGGAGTGTGA TCTAAGACAT 480
CAACTTTGGG CGATTAGAGG CAGTCGGCTT CAAACTGAAG GAGCCATTTT TCCTTCAGTG 540
CCCAGCTCAA TGTCTGGCAC ATAGTAGTTG CTCAGGAAAT ATTTGTTTCA AAAAAATGAA 600
AGTGTCAATG TCAGTGTTGT AGGATTTTTA AAGATGTTGT AGGACTCTCT CTGTAGTTCA 660
GCTAAGAGCT GGATCATTGT CACACGGCCA CAAAAAATTA GGCTTGCAGA CAATTTGAAG 720
GGTGAGGAAG GCAGGGTTTA TTGGGTGAAA CGGAAAAAAG GGAAACAGAG ACCCTCCGCA 780
AGGTCAGAGT TCTCCTGACA TGCTTCCTGC CTCACAAATT GAATCCCAGG TTCCACCCAG 840
GAACAGGAGG GGCCAGGCTC CTCCCCGCTG CAAATGGTGG CAGTTTCTGT GGCTCCACCC 900
CAGTGCACAC TCCTCCCAGT GGGCAGGCTA GTTGGAGTTT TTTTTGGGGA CCCCCTTACA 960
CTTGACTGTC TCATTAGGTC CTGCAACTCA GTACTCCCTC CCAAAGGTGA GGGACCAGGG 1020
AGTGCAGAGA GGTGCAGGGG GCTGATTTTA TTTTATACAG GTGGTCAGAG GAGGACACAC 1080
AGGTAAAGTG ACATTTGAGC AAAGACTGAG 1110
|
