| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00718 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:15294650-15295950 |
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 | CTAGATGGTC CCATCTAGGG GTGACGGGAG ACAGTGACAG ATCATCAGGC ATTAGATTCT 60
AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT CACAAGAGGG TTCGTGCTCC 120
TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG TGGAGCTCCG GCGGTAATGT 180
GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC TCGCTCGCCC CTCACCTCCT 240
GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC AGTCCATGGC CTGGGGCTTG 300
GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA CAACAAGAAT GGGAAACGAA 360
CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC TGCCCTCTCT CAGGGCTTAG 420
GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA GGGCACAGCA GCCAGCACGG 480
GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG AAGAAAGGAT CCGGAGTTTC 540
CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT CCCTGCCACA GAGTGAGTCA 600
CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT TTGCTCATTC ACCAAATGTT 660
CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT GTGGTTCAGA GCATTCCAGG 720
CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA CACTCAGTGT ACCTTACTTG 780
AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA GAGTCTATCC CATAGGCATT 840
CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC 900
TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG CTGCCTTTGC AGATGTCACC 960
AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT GTTGAATAGA ACGATGTGTC 1020
ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC ACACATCCTT GTCACCACAG 1080
CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT CCCTTCCCAC ATCCGCACTC 1140
CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC TTCTATGCAG TTCATCACCT 1200
GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG CTTGAAGCTA CTGCTGTTTC 1260
TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1300
|
