| Tag | Content |
|---|
EnhancerAtlas ID | HS031-13694 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr20:5668560-5669710 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09377 | chr20:5666802-5670926 | CD14 | | SE_58609 | chr20:5622683-5700446 | Ly1 | | SE_60511 | chr20:5614796-5674594 | DHL6 |
|
| | 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 |
| GH20I005687 | chr20 | 5668448 | 5670445 |
|
Enhancer Sequence | TCCTTCTCCT GAGAATAACT GAGCTGCTGC TAACATGAAG ATGGTTTAGG GCAAAAATTT 60
TAAAAAGGCA CTCCCTTTGG GTAGACAAAT TGCAAAATTC GTGCCCACTC CATGTGATGA 120
ATTACAGACA GTTTGCACCT TCCCCTTCCT GCTCATGCAA GGAAGTGTTG CGCCCTTCCT 180
CTTTCCCTTT GTGTCTGCTT GGAATTGGGT CTGATTGGAA TTGGGTTTCG TCACTTGCAA 240
CCAAAGAATC CTGACTGACA TAGATGGTAC TTGGCGCCAT GAATTAATGT GTTGCCTCTC 300
ATAACTAATT TCCTGGAGGT AATCCATTCA CTTGAATGAA GATTGGAGCA CTGTGACCAG 360
CAGTGCAACT TTATGGCTTT GGCTGTTAGG GATCTCCATG CCCCCTAGGT CCAGTTTAGG 420
CTGCTCCCTG TTAGACCTGT AGCAGGTGCT CTTCTTGCCC ACCATGTCCC CTCACTCTGA 480
CCTCTCCATC GGGCGGGGCC CTACTCATGG CCCCTTGGAA GTAGGGGCCC TTATTTCCTC 540
ACAAGAGGAA GCCAGCTGCT CAAGGGCTTC CTCTTGCTGC CAGAGCCCAC TTTACCCCCA 600
ACGTGGCAGG CCAGAGTGTC CAGGACTTGG CCCCACACCG GAAGCAGCCC TTGCTGCCTG 660
ACTGATGGGG GGTGGTATGT TCAACACTCC AGCCGCCTTT CCCGGCAGAG GCAGCGTGCA 720
GAGGTGTGTT CCACACTGGC TCCCAGAGGT GCCCTGAGGA CAAATGCAGC TCAGCTCCCT 780
TTCTCCCCAG TCCCTTAATT AGCTACTCTC TGTCTCAGTC TCCGCCCTCC CCACCGCTCT 840
GCCCCCGCTC CCTTTTCCCG TCCTCCCCAC GGGTGTTTCC TGGAGTCACC TCCCACATAA 900
GCTACTTGCA CAAGAGTCCT TGTCTCAGAG TCAGCTTCTA GGGGTTTCCA CCTTAACATA 960
AGACCTATGC CCAGGGTCAT CACATGAAGA CCTGAGTCAG CCACTTACTG GCCAGATGGC 1020
CACGGGTTAC CCACTCTGGG CCACGGGTTA CCCACTCTGG GTCACAGGTT ACCCACTCTG 1080
GCCCTCAGTT TCTGTCTGGA AAGAGGTAGC CAGTCACACT AAAGGGGGAC TTCTTTTTGG 1140
GTAGGCTATT 1150
|
