| Tag | Content |
|---|
EnhancerAtlas ID | HS170-02552 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr22:25030570-25031450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr22:25031041-25031053 | GGGCACGTGGCT | - | 6.18 | | STAT3 | MA0144.2 | chr22:25030590-25030601 | CTTCCCAGAAA | - | 6.02 |
|
| | 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 |
| GH22I024634 | chr22 | 25030768 | 25031567 |
|
Enhancer Sequence | CCTGCCAGCC ACCTGGTCTG CTTCCCAGAA ATTCTGTCTT GCAGGCTGTT GGGAGGATCC 60
CAGTACTTTG TAAACTAAAG CAAGGGAGGA GTGGCCGTTC TCTCTGTTCA TTCATTCACC 120
TTTTCATTCA TTCCTTCTTC CCTCCATTCC CCCATCTGTC CATCCTTCCC TGCCCTGATT 180
GCTCATGCCA CCGCCCCCCG CAGCCCCTCC TGACCTGGTC CTTTGGTTTC TCTTCAGGGA 240
TTTCTGTCTC CTCCCACAGG GCTGAGAATG GCAGCTCAGG GACAAGTAGG GGCTGGGGAC 300
TGCTTAGTCT CCCCAGTGGC TCTCAGGGGA TTTGAGGGTT TGACGCCAGC TGCCACCCCA 360
GGCTGTGCCC CTCCTCTGCT CAGGAGGACA TACAGGATGC AACACCCACT TAAACTCGAA 420
GTTGCAAAGA TGCAAATGAG ACTGGGGTCT CAGGCACCAG AGACCACCCG TGGGCACGTG 480
GCTTTTGGGA TTGGAGACCT GCTGCCACAG ATCTCTGAAG AGTCTGGACC TGCTGGGTCT 540
CCCCAAGTGA CTCTCTGGGG GTCTCCATAG CATGCCCTGC TGTGTGCATG ACGGTCACTG 600
GTTGGGTAGG GGTCTCTACT CTAAAGCTCC CTCTGCCGGC ATCCCCTCGA ACTCTCCCTT 660
GGTGAAGAGA GAGGATGTGG TTTGCCCCAG TGTTTTATCA AACAACTCTC TCCACTTCCT 720
GTTTTAAGAA GCTGGGAGTG GAAGAGAGCC TGGGGCTGGC CCCAGCTGCT GCTGCGAAAC 780
AGGGGTCACT GGACGCTGGG ACCCTGGCCG GGCTGGCTGG AGGCCTCAGG AAGAGGCCTG 840
CTACAGTGTC ATCCTGGCCA AGATTCCTCC CTGCAGAGGA 880
|
