| Tag | Content |
|---|
EnhancerAtlas ID | HS047-33463 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:134461510-134462810 |
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: 2 | ID | Chromosome | Start | End |
| GH08I133447 | chr8 | 134460082 | 134462243 | | GH08I133450 | chr8 | 134462621 | 134462728 |
|
Enhancer Sequence | AGAAATCACT GCAGAGTCAA GGATGAAGGG TGGGAGAGGG AGGCCAAGTA GAAACACCAA 60
GGTGTGGAGG TCTGGGCAGG CAGGAGCCGG TGGTGCCACG TGGCCCTGTG AAGCCGTGGG 120
CAGCTGGTCA GACACTCACC CTTGCTTGGG GCTTTGACAT TTTCCAACTG GACACAGACT 180
TCTTCTCAAT CTATTTTGTT AGCTGGATGA CAGAGATATA ATCTCCTCAT CTGGAAGGTG 240
TTGTCCTTGT TACTATCTAA GATCAAGTTC TTTTAAGTTC TGGCCTTACA CGTGGGTGTG 300
TGGCTTTTCC CTTGAGGTTT TCAGCTTGTG TCTGGTTCCC AACCAAACCC CATGTTGAAT 360
CTGGTGGAAG GTGGGTCCGT TGCGCCCTCT GGTGGCCACC ATCACCAGGC GCTCTTGGCC 420
AAGGTCCTAA TGAATAAACC TGGCCGTTGG GCCGGACCAG CTCTGTCGCC GTGAGCCAGC 480
CATGGGCACT CATCTTCAAA GTGCTTTTCT CTGGAGCAAC ACCGTCCCCT GTCCCCACAC 540
CCCTGGGGAG TATGGCGCAC TTGCAATCTT TACCCGGGAC TCAGGAACCC CAGCCCTTGC 600
GATTTAAGTT CTGGCTACAT CCCTAACCCC CTGGTAAGTC ACTTAACCTC CTTGAGTGAA 660
GCTCAGTTTC CTCTTTAAAT TCCCCTCTCG AGAGACCAAT GCCTCTTGGC AGGATTGTTG 720
CAGGATTAAA CGAGCTTAAT GGAGGTAAAG CACTCAGCCC CCGTTGCCAG CGTGTGAAAA 780
AGAACCAGCC GCGGTCATTA AAAGCTCCTT TATTTCATGG GTGTTGCAGC TGTCTGGCTG 840
CCCGCCCGTC CCCCCACTAA CTCTCACACT CTGGTGGCAG AGACCTTCTC TTGCCCATCT 900
CTGTATCTCT AGTCCCCATG GCCCTCAGTG CGTATTTGCC AAGTGAAATA TATACATAAA 960
GCACATTCGC TTATCACAGT CCTGTGAGGC AGACACCCCC GGAATCACTG TTCCCGGTTT 1020
GCAGAGAGGG TCTATCCGTG GACCCCGGTC TTTGACTGCT GGGGCCTGTG ACTGTCCATG 1080
GGTGTCCATG ACCCAGTCAT GGCGCCCTCT AACGCATCCT CTCTAACTTC AACCCGGCCC 1140
TCCACCCTAG CCACCAGCTG CCTGTACTCA CAGTCATTTT CTCCGACGGT TCACAGTCCA 1200
TGGGAAAACG TTCCTCCATT GTTCTCTCCT CCTGCCTTCG CCTCAGCTCA GCATTTTATC 1260
TCCCCAACTC TAGGGGAAAA GGAAGCTATC AGACGGCAAT 1300
|
