| Tag | Content |
|---|
EnhancerAtlas ID | HS191-00301 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr1:15294630-15296010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26798 | chr1:15294684-15296104 | Esophagus | | SE_53292 | chr1:15293321-15296336 | Spleen |
|
| | 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 |
| GH01I014967 | chr1 | 15294172 | 15298701 |
|
Enhancer Sequence | CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG ACAGTGACAG 60
ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT 120
CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG 180
TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC 240
TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC 300
AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA 360
CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC 420
TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA 480
GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG 540
AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT 600
CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT 660
TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT 720
GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA 780
CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA 840
GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG 900
TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG 960
CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT 1020
GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC 1080
ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT 1140
CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC 1200
TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG 1260
CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1320
CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT GGTAAATCTC 1380
|
