| Tag | Content |
|---|
EnhancerAtlas ID | HS176-34911 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr6:85231050-85232530 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:85231192-85231204 | ATGTAAACAGAT | + | 6.62 | | FOXP2 | MA0593.1 | chr6:85231192-85231203 | ATGTAAACAGA | + | 6.02 | | Foxa2 | MA0047.2 | chr6:85231976-85231988 | CCAATGTAAACA | - | 6.62 | | SOX10 | MA0442.2 | chr6:85232134-85232145 | AAAACAAAGAA | + | 6.62 |
|
| | 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 |
| GH06I084521 | chr6 | 85231317 | 85232615 |
|
Enhancer Sequence | TGAAACTATA ATTGGCCTCT CAAATGTGGT AGTGAGAGAT CTGGCTTAGT GACAGAAAGA 60
CCAAAATCAG TAAATGAGGG AAAATAACAA CCTAGAGAAT AATGACTGAA AGAAGAACAT 120
TAATACTAAA TAATGAAGAA GAATGTAAAC AGATAAGAGA CTCAGAAAGC CCTAGATCTT 180
TAAAAGGCTG AAAGAGGGAG GGCAAAGATA AAAAATGATA AGACCTGTCA AGAAGAACAA 240
AGTCAATGTG TGTACATTAT TCAGTTTAAG GAATTAGAGT CACAAGGTCA AGTGTGGGTA 300
ACAGTAAATA TGAATGATGA GGAATAAAAT AAGTAAAAAG CAAGCTAGTT TCATAAATCA 360
ATTCCACAGC AACTTAGCTG GGGGGAGGTG AAAGGAGAAT GGAGGATAAC CCATTGGAGC 420
CTGTTGAAAT GTCAAGATCT ATTACCAATT ACTAAATATC AACGTGTTCA TGCAAAATCC 480
CAGTGTTCAG GGTCATAAAA CAGTGCATTC CATGGACCAG TGGGGATTAT CTAATTTGCA 540
CTTTGAAGTG CACTTAAACA AAACAAGAGA AAACATGGGC ATTTGTAGCA AGAGGAAAAC 600
ATACATTAGA AGATAAGTAG AATGAAAGAA CATATAAGCC CCCATCTCAG CCTATTATCC 660
CAGGATGGTC TCTGAGCCCA CCTTGGAGGG GACCCCATTT CTGCTTCTTT GGCTGTACAA 720
TGCCAAGGAA GAAGCTGCTA TAAAAGACAA GCAAAGGGGG AGGTCTGGAA TGAAGATTTG 780
GGCAAGAGTC CATACGCCAA GGTTAAGGGC CAGAACTTCT GCTCTTTGCA CTCTCCCACT 840
GGGAGCTGTA CAGGCAGGAG AAACAGGGAT GGGCCCCTTG GGGAAGAAGG GGACACTAGA 900
GTTGGCCACT AACAACAGAT TAAAGCCCAA TGTAAACAGT GTGCTGGACA CATGTGGGTT 960
GTAGAGAGAG TGGTGATGAA TAAGCCTGTA TCCAGGCAAG GACTTCAAAC AGGAGGAGGC 1020
TGAGCAATGA TGAAAATGAT TCAGTGCCCT CAGAAATGAC TCATGAGAGG AACAGAATGT 1080
GAAGAAAACA AAGAAGAAAT GTCCACATTT ATCAAGCACT TGACAAATGA TGGGGGATGC 1140
ACAATTAGGG AGAGCAAATC ATTGGAACAG AGTAAAGACA AGAAGGGAGG CCATAGGCAG 1200
TCTGAAAAGA AGAAATCCAG GGATGCAAGG GCAGCAGTAT CATAGAGTGG ATTAATCCGC 1260
TCTCACTGAA TTATGGTCAA CACAAATTAA TCTTGCAGTC CAATTGATTT AACACTGAAC 1320
TGGACTGTAA AATTCAGGGA ATGCTGATTC TGTTTGACTA GCATTGGTCT CTACCTATTT 1380
TGTGAACATC TCCATTCTCA GGCTCTTTCT CCCTTTAGGT AGGGCTGATC TCCAGCAGGT 1440
CTGCTCTGGT AGAGCCTAAT CAGGTATATG CCGATGCCAT 1480
|
