| Tag | Content |
|---|
EnhancerAtlas ID | HS108-40525 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:33506220-33507370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr9:33506301-33506311 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr9:33506682-33506692 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr9:33506301-33506311 | GGCACGTGCC | - | 6.02 | | HES2 | MA0616.2 | chr9:33506682-33506692 | GGCACGTGCC | - | 6.02 | | IRF1 | MA0050.2 | chr9:33506960-33506981 | ATACCAAAACTGAAACTGGGA | - | 6.27 | | IRF9 | MA0653.1 | chr9:33506962-33506977 | ACCAAAACTGAAACT | + | 6.46 |
|
| | 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 |
| GH09I033505 | chr9 | 33505945 | 33508270 |
|
Enhancer Sequence | GGCCAGGAGT TCAGAGACCA GTCTGGGTAA TGTAGCAAGA CCTCATCTCT ACACAAAAAT 60
GTTTAATTAG CTTAGTGTGA TGGCACGTGC CTGTATTCCC AGCTACTCAG GAGGCAGAGG 120
CAGAAGGACA GCTTGAGCTC AGGAATTCAA GGCTGCAGTG AACTATAATG GTGCCATTGC 180
ACTCAAGTCT GGGTGAAAGA GTAAGGCTCT GTGCCCCCAG GTCCAAAAAG AAGAAAAAAA 240
AAGAAAAGAA TTTAGGCAGG AAACTTTTCT ATTGCTCTTA AAAGTAATAA GGCCTAGAAA 300
TGCAGAGGAT GAGGTCAGGC ATGAAGGCTC ACGCCTGTAA CCCCAACACT TTGGGAGGCT 360
GAGGCAGGTG GATCACTTTA GCCCAGGAGT TCAAGACCAG CCTTTGTAAC AGGGCGAAAC 420
CCTGTCTCTG TGAAAAAAAA GCACAATTTC GTCAGATGTG GTGGCACGTG CCTATAGCCC 480
CAGTGACTTG GGGGGCTGGG GTGGGTGAAT CACTTGAGCT CAGGAGGCGG AGGTTGCAGT 540
GACCCAAGAT CACATCACTG CATTCCAGCC AGGGCAACAG AGTGAGACCT TGTCTCAAAA 600
AAAAGAAAAT GTAGAAGATG GTATGACTCA TGTTTTTTCA GGGGTTTCAA GTATGTATCA 660
AGGCACTAGA TAACTTGACT CTGGAATTTC CTAGGAGTGT AGATATGCTG TCTTCCTGAC 720
TGAATAACCC TATTATTCAC ATACCAAAAC TGAAACTGGG ATAAGCAAAT TTGACAATAA 780
GCCCTGTCAC CCAGTCCTTT CCTTTCCTAA TTTGTAGCTT CCATTTGTGT AATCAGGCCT 840
AAAATCCCTT TTTTGAGTAG GTATACAGCA GAAAAGCAAA CATTCAAAGC AGTACAGAGT 900
TAGAATTTAA CACATAATAC GTAAGAGCAG AGTTTCTTAA CTCAGCACTA CTGACGTTTT 960
GAACCAGATA CTTCTCTGTT GGGCAGGACT GTCCTGGCCA TTATGGGCTG TTTCGTAGCA 1020
CCTCCTGGTT TATACTCATT AGATGTCAGT AGCTCATCCC CCATCCACCA ATCATGATAA 1080
TCAAAAATCT CTTCAAACAT TGCCTAAAGT TTCCTGGGAC ACAATTGTTT CCAGTTAAGA 1140
ACCACTGCTT 1150
|
