| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04465 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:82201270-82201940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr10:82201882-82201897 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr10:82201882-82201900 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
|
| | 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 |
| GH10I080441 | chr10 | 82201661 | 82201850 |
|
Enhancer Sequence | CACACAAGTA GAAGAAATTC AGGAGCAGAC CCTCACAAGC AGAAAAAATT CAGGAGCAGG 60
CCCACTGGCT GCAGACAGTG GGGCCACCTG AAGGATCCTT CTTAGACTTC CATAGCGACT 120
TCTTAACTGG ATCGCTGTGT CCAAGGCTAG GTCATGCTCC AGGCAGCCCT GGTTATTCTG 180
CAGTTGTAGG GGTCCTCCTG GGCCTCGTGA AATGGATTCT GGCTATGGCT TAATGATGTC 240
TCACTGGGAT TGTGTCAGTT AAAGTGTTCT CGAACTAATG AGACAGACCA AACCCCTGCC 300
TCCAAATCCA GGGAGGTTGG TGGGATATGA AATTGACCAG CTTCGCTAAG GGGGATATCT 360
GGGTTTCGGA TGGACTACAG AGCAGTTCTC CAGATGGCCT TGGACTGACC CAGTTCTCCC 420
AGCTTTCTCA CTGTAGTTCT CAAGAATAAC TGTAGAATGT GCTGGGAATG CAATAGCCTG 480
AGGTCAGGAG GAACTGGCCA GAACAGCCTG GGCTTGTTCC TGTCCCTGCT ATGAAAGAAT 540
GCCCTTCAGG CCCGGAGAGG CGGCTCACGC CTATAATCCC AGCACTTTGG GAGGCCAAGG 600
GGCAGATCAC CCGAGGTCAA GAGTTCAAGA CCAGTTGGCC AACATGGTGA AACCCTATCT 660
CTACTAAAAA 670
|
