| Tag | Content |
|---|
EnhancerAtlas ID | HS141-11488 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr20:5668240-5669550 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr20:5668341-5668354 | ATGACCTCATCTT | - | 6.54 | | JUND(var.2) | MA0492.1 | chr20:5668340-5668355 | TATGACCTCATCTTA | - | 7.07 |
|
| | 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 | CTCCCAAAGT GCTGGAATTA CAGGCATGAG CCACTGCACC TGGCCTCTTC CCCTCTTACA 60
AAGACACCAG TCATATTGGA TTAGGGCCCA TTTAATCCAG TATGACCTCA TCTTAACCTG 120
ATTGCATCTG CAGGGACCCT ATTTCCAAAT AAGATCACAT TCACAGGTCC CAGGGGTTGG 180
GACCTTAACA TATCTGCTTG AGGGACGCAG TTTAGCCCAC AACAGTTACC ATTCCGTCGT 240
GGGCTTATTT TCTGCTGGGT GGCAGCTACT TTATCTGTCA CAGTTTTGAG GAGGACACTT 300
GTCATTCTGT GTGCCTGGTA TCCTTCTCCT GAGAATAACT GAGCTGCTGC TAACATGAAG 360
ATGGTTTAGG GCAAAAATTT TAAAAAGGCA CTCCCTTTGG GTAGACAAAT TGCAAAATTC 420
GTGCCCACTC CATGTGATGA ATTACAGACA GTTTGCACCT TCCCCTTCCT GCTCATGCAA 480
GGAAGTGTTG CGCCCTTCCT CTTTCCCTTT GTGTCTGCTT GGAATTGGGT CTGATTGGAA 540
TTGGGTTTCG TCACTTGCAA CCAAAGAATC CTGACTGACA TAGATGGTAC TTGGCGCCAT 600
GAATTAATGT GTTGCCTCTC ATAACTAATT TCCTGGAGGT AATCCATTCA CTTGAATGAA 660
GATTGGAGCA CTGTGACCAG CAGTGCAACT TTATGGCTTT GGCTGTTAGG GATCTCCATG 720
CCCCCTAGGT CCAGTTTAGG CTGCTCCCTG TTAGACCTGT AGCAGGTGCT CTTCTTGCCC 780
ACCATGTCCC CTCACTCTGA CCTCTCCATC GGGCGGGGCC CTACTCATGG CCCCTTGGAA 840
GTAGGGGCCC TTATTTCCTC ACAAGAGGAA GCCAGCTGCT CAAGGGCTTC CTCTTGCTGC 900
CAGAGCCCAC TTTACCCCCA ACGTGGCAGG CCAGAGTGTC CAGGACTTGG CCCCACACCG 960
GAAGCAGCCC TTGCTGCCTG ACTGATGGGG GGTGGTATGT TCAACACTCC AGCCGCCTTT 1020
CCCGGCAGAG GCAGCGTGCA GAGGTGTGTT CCACACTGGC TCCCAGAGGT GCCCTGAGGA 1080
CAAATGCAGC TCAGCTCCCT TTCTCCCCAG TCCCTTAATT AGCTACTCTC TGTCTCAGTC 1140
TCCGCCCTCC CCACCGCTCT GCCCCCGCTC CCTTTTCCCG TCCTCCCCAC GGGTGTTTCC 1200
TGGAGTCACC TCCCACATAA GCTACTTGCA CAAGAGTCCT TGTCTCAGAG TCAGCTTCTA 1260
GGGGTTTCCA CCTTAACATA AGACCTATGC CCAGGGTCAT CACATGAAGA 1310
|
