| Tag | Content |
|---|
EnhancerAtlas ID | HS082-00236 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:15294560-15295980 |
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 | ATTATTATTA CATTGTAATA TATAGTGAAA TAATTATACA ATTCACCCTA ATGTAGAATC 60
AGTGGGAGAC CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG 120
ACAGTGACAG ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC 180
ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC 240
AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT 300
GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG 360
GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT 420
CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG 480
CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA 540
AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG 600
CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG 660
GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT 720
ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT 780
GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA 840
ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC 900
CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA 960
CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC 1020
CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC 1080
CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC 1140
TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG 1200
TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA 1260
CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA 1320
AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA 1380
GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT 1420
|
