| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00316 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:15294690-15296180 |
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 | ATCATCAGGC ATTAGATTCT AATAAGGAGC ACGCAACCTG GATCCCTCAC ATGCGCAGTT 60
CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC GCTGCTGATC AGACAGGAGG 120
TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT AAATACAGAT GAAACTTCGC 180
TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA AGAGGCCAGG GACCAGTACC 240
AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC TGCATTGTGT CACTTTGTTA 300
CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG GACTTGGCAG CCCTAAACAC 360
TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT TTCCTTTAGA AACGCCTGCA 420
GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC ACTGACTGAG CATGGAGCAG 480
AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT AAGGCCTGTG GGAGCCTTTT 540
CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA ACACAACTTT ATTATTTAAT 600
TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC CAAAGCTTGT GCCGATGCCT 660
GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA CATGCCTGAA ACCTACGACA 720
CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG CCAACCAGGC CTGTAGATGA 780
GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG 840
TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG CAGGTGCAGC CATGCCCTGG 900
CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT 960
GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT GCCCACTTGC TTTCTTAGAC 1020
ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG CTACTTGATG TTTCCTGTGT 1080
CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT CCATCAAAGA CGTGTTCATC 1140
TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC CTCTTTAGTA AATTCATACG 1200
CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC 1260
CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG ACTCTTTGCT GGTAAATCTC 1320
GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA CAGAATGTCT TCCTTACATA 1380
CTACCGGCTG CTTTTAAATA TTGTTAACAG ATCCCCCTTA AAGGCTTCTT AGACTCCACA 1440
TTTTGATCCA GTTGATAATA ATTGATGGTC AGGTGGAAGA ATTGCCCAGG 1490
|
