| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26454 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:20960280-20961210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr22:20960358-20960373 | GGGCCAGGCTGACCC | - | 6.25 | | IRF1 | MA0050.2 | chr22:20960865-20960886 | AAACTGAAACAGAAAGAACAA | - | 6.97 |
|
| | 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 |
| GH22I020606 | chr22 | 20960382 | 20961659 |
|
Enhancer Sequence | CCCATTCTAG GGCCTGGCGA AGTTGAGCCT AGGAAGGGCT GGTCTGTGCT CCACTCAGCA 60
GCAGCTGGGA GAGGGCCAGG GCCAGGCTGA CCCCAGCACA GGCCGCTGTC TTGGCCTCCA 120
CCCACTGGAG CAACATTTGC CCAGGGGAGC CAGTGGCATG TGAGGAGAGG GGGCCAGGGC 180
TCACCATTTC TCAGACACAC TGGGGCTGGG AGTTGCTGCT GGCAGCCTGC TTGTCAGCTG 240
CATACCACCA TGGCTGCAGG TAGCTCAGCC ACACCTCCAG GACCTGTGGG GGAGGTGTGT 300
GCTGAAGGCC CAGTGGCTGG GGCCAAATCC TCTGATGGCC TGGAACCCAG GTACCCAGGT 360
GGCAGCTAAG TTGGCTCTTC CCACGTCCCC CAGAGGGCGC AGGAGAGACG CGCACAGCCC 420
TGTGAGATTT GGTTCTCTCA CTGCTCTTCA GAAGCCAGGG TCATGGGCGG GCTCTTCCCG 480
GCCCACGGGA CCCAGTGCTA CCTGGTTGCG TAAGAGTAGA AACCTGTCTG GCACCAGACA 540
GGTGGGATGG GGCAGGGCTT TGCTGTGCCT GAGGGTTGCC TTTGGAAACT GAAACAGAAA 600
GAACAACGTG GCCCTCCAAG GCCCCCTCCT CTCCAAGGTC TCTGTGACAA CACTTGTTCT 660
CCTTCATCCA CCCCAGGGGA CCTCCCTCAT TGGGGCACAC AGAAGACACA GGCACACATG 720
TGATGGGGCC GACACTCCTA GCTCTGAACA ATGCGTCCAA GGGCCAGTGG CCAAAGCAAT 780
GCCGCAGGAA GAGGTAGAGT TTCTGCTGGA CTAACCTCGG GACAGCGGCC TGCAGAGGAG 840
GGGAGGGTCA CCAGCCGCTT GCACAGTAAG GTGGCCCTGC TCACAGATGA GCCCGGGGTT 900
CCCATTAGTG AGGGTTGGCT CTGCTGGGAG 930
|
