| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00458 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:15294570-15296050 |
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 | CATTGTAATA TATAGTGAAA TAATTATACA ATTCACCCTA ATGTAGAATC AGTGGGAGAC 60
CTGAGCTTGT TTTCCTGCAA CTAGATGGTC CCATCTAGGG GTGACGGGAG ACAGTGACAG 120
ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT 180
CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG 240
TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC 300
TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC 360
AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA 420
CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC 480
TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA 540
GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG 600
AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT 660
CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT 720
TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT 780
GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA 840
CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA 900
GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG 960
TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG 1020
CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT 1080
GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC 1140
ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT 1200
CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC 1260
TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG 1320
CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1380
CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT GGTAAATCTC 1440
GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA 1480
|
