| Tag | Content |
|---|
EnhancerAtlas ID | HS047-32181 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:8639420-8640800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr8:8640143-8640158 | CCAGGTCAAAGGTCA | + | 7.36 | | NRF1 | MA0506.1 | chr8:8640037-8640048 | TGCGCATGCGC | - | 6.32 | | Nr2f6 | MA0677.1 | chr8:8640144-8640158 | CAGGTCAAAGGTCA | + | 7.73 | | Rxra | MA0512.2 | chr8:8640144-8640158 | CAGGTCAAAGGTCA | + | 7.58 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr8 | 8639524 | 8639621 | | chr8 | 8640001 | 8640594 | | chr8 | 8640652 | 8640764 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I008782 | chr8 | 8639724 | 8641837 |
|
Enhancer Sequence | GCGAGCGAGG GCTGTGAGGA GGGCCAGCAC GCTGTCACCT CTCAGCGGGA TGCAGCCGTA 60
GGGCCAGCCA CACCTCTCCC ACGTGGGACG CACCTCTTGT GACACTTCTT TTGGAAATTC 120
TAGTTGCCTC CTGCTTTCCT CTGTTCTGTT GGCAAAAGTG GCTTTGAATT CTGCACACCC 180
CACGGTTCTA CCTGCCTTGT CAGGAGTCTT GCAGTGAGGC CCTCCTGGTC TGAAGCGATC 240
CCTTCTTCCC TGTATTGCGC TGTCTTCAGG GCAGGGCTCC TCTTGTTACA GTAGGTAGTC 300
AGGCACACAT AAGCAGGGCA GAAGAACGCC CCCCAGCAAC CATCAGGTGA GATGGTCAGG 360
TGGTTGTTAC ACTGTCTCTC TAAAATAATT GGTGACAGCC GGTGCCAGGG AAAGGCAGGC 420
TCCCAACAGA CAGAAAACAC CTGAAGCTGG TGATCAGCAG CTTTCGGATA AGAGCTCAGG 480
ATTTGGGTGC GTGGGCTGAA GCATGCGCAT TAAGAGGCAA AAGGACGGCG CTTGACTGGT 540
ATAGGACCTT CTAGGAACAT TCAACTAGTA AGGGAAGAAC ACCTCAAGTG AGCATGCGCA 600
CAACTCCAGT AATACACTGC GCATGCGCCC CCTCCCAAGC GCTGGCAGGC CTCTGCGTAT 660
GTGGACGGCC AACCCCAAGG AAGAATCAGG GGAGACCTCG GAAAAATGCC CACGTATAAA 720
ACCCCAGGTC AAAGGTCAAA CTGTGCACTT GCTCTCTCAA GCCGCCTGCT TGGCCCTCTT 780
CCAAGTGTAC TTCCTTTCGT TCCTGTTCTA AAGCTTTTTA ATAAACTTTC CCTCCTGCCC 840
TAAAACTTGC CTCCGTCTCT CCTGCTGTCT TATGCCCCTC GCTTGAATTC TTTCTTCTGA 900
GGAGGCAAGA ATTGAGGTTG CTGCAGACCC GTTATGGATT CACCACGTTA ACACCCTGGC 960
TTTGGTCCTT CCTTATCTTC TCTTTGCCTT TATTTAAACA ATATGGAGTA CTAAATCCTC 1020
TGATGGGTAC CTGAGGGGCC TGCTCTTCCA GTTTGCAAAT AGGGCACCCT GAGGCAGTAT 1080
GTAGCAGGAC TTCTGCTAAG AGCCTTTGAA AGAAAGATCA GGGGAACTTC CAAAGCTACC 1140
ATAAATTCAA CAGCTGTGAC TTAGGAATAT AGTGGATCAT TGAAAAAAAA AAAAAGATTC 1200
TGATTTAAGA GAGCTGATCT TCAAGTTATA TCCTCAGCCT GAAAACAGAG GCAGTTTTAA 1260
AACAGGGATT CTTTAGTTTT CTCTTCGGAG ACCAAACAGA TGAGAGCTAC CACCACCCAC 1320
CTCCCACAGC TCCAACAGTA CCACTAAGGA CTAAAACTAT AAAAGTCATT CCTTAACTGA 1380
|
