| Tag | Content |
|---|
EnhancerAtlas ID | HS105-79859 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:134461230-134462400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:134461889-134461908 | TTGCGCCCTCTGGTGGCCA | - | 8.69 | | GFI1 | MA0038.2 | chr8:134461511-134461523 | GAAATCACTGCA | + | 6.74 |
|
| | 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 |
| GH08I133447 | chr8 | 134460082 | 134462243 |
|
Enhancer Sequence | TAACCCTGGT TGATCAGTTA TGAACTGTGG CTACAGACAC ATAACTAATA GTCTCTGTGC 60
CTCAGATCTT CCATGAGGAT ACCACCCCCA TGTCATTCAT GGGGGTTGTT GTGAGAATTA 120
AAGGAGAAAA TGCGTGTGAA ATGCTTGGCA CACAGAAAGG ACTCAGAAAA GTCTGCCTGC 180
CGTCTTTCCT TAATATATAC TATGTCACCT TATACCCATT TTATAGATTA AGAAACTGAG 240
GTTCAAAGAA GTCAGGTTTT CCCCATTGGT CACACAGCTA AGAAATCACT GCAGAGTCAA 300
GGATGAAGGG TGGGAGAGGG AGGCCAAGTA GAAACACCAA GGTGTGGAGG TCTGGGCAGG 360
CAGGAGCCGG TGGTGCCACG TGGCCCTGTG AAGCCGTGGG CAGCTGGTCA GACACTCACC 420
CTTGCTTGGG GCTTTGACAT TTTCCAACTG GACACAGACT TCTTCTCAAT CTATTTTGTT 480
AGCTGGATGA CAGAGATATA ATCTCCTCAT CTGGAAGGTG TTGTCCTTGT TACTATCTAA 540
GATCAAGTTC TTTTAAGTTC TGGCCTTACA CGTGGGTGTG TGGCTTTTCC CTTGAGGTTT 600
TCAGCTTGTG TCTGGTTCCC AACCAAACCC CATGTTGAAT CTGGTGGAAG GTGGGTCCGT 660
TGCGCCCTCT GGTGGCCACC ATCACCAGGC GCTCTTGGCC AAGGTCCTAA TGAATAAACC 720
TGGCCGTTGG GCCGGACCAG CTCTGTCGCC GTGAGCCAGC CATGGGCACT CATCTTCAAA 780
GTGCTTTTCT CTGGAGCAAC ACCGTCCCCT GTCCCCACAC CCCTGGGGAG TATGGCGCAC 840
TTGCAATCTT TACCCGGGAC TCAGGAACCC CAGCCCTTGC GATTTAAGTT CTGGCTACAT 900
CCCTAACCCC CTGGTAAGTC ACTTAACCTC CTTGAGTGAA GCTCAGTTTC CTCTTTAAAT 960
TCCCCTCTCG AGAGACCAAT GCCTCTTGGC AGGATTGTTG CAGGATTAAA CGAGCTTAAT 1020
GGAGGTAAAG CACTCAGCCC CCGTTGCCAG CGTGTGAAAA AGAACCAGCC GCGGTCATTA 1080
AAAGCTCCTT TATTTCATGG GTGTTGCAGC TGTCTGGCTG CCCGCCCGTC CCCCCACTAA 1140
CTCTCACACT CTGGTGGCAG AGACCTTCTC 1170
|
