| Tag | Content |
|---|
EnhancerAtlas ID | HS139-11177 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:126354580-126355850 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr11:126354611-126354622 | GATTTAATTAA | + | 6.02 | | USF1 | MA0093.2 | chr11:126355361-126355372 | GCCACGTGACC | + | 6.62 | | USF2 | MA0526.2 | chr11:126355359-126355375 | TGGCCACGTGACCATG | - | 7.36 |
|
| | 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 |
| GH11I126483 | chr11 | 126353546 | 126355346 |
|
Enhancer Sequence | AATCCTGTAG ATGTGTTAAT TACATATATG TGATTTAATT AATGTAGGTG TGCTTTCCCC 60
CTCTTCAGAC CCTCCCCGCC TCCACTTAGG TCTATATTAA GAAGATGTGG GGCAAGATGC 120
AAATGGGATT TTTTTTTTTT TTTTTCTGAG ACGGAGTCTC GCTCTTGTCA CCCAGGCTGG 180
AGTGCAATGG CACAATGTAG GCTCACTGCA GCCTCCGCCT CCCAGGTTCA AGCGATTCTC 240
CTGCCTCAGC CTTTTAAATA GCTGGGATTA CAGGCACCTG CCACCACGCC TGGCTGATAT 300
TTTTTGGTAC TTTTGGTGGA GACGGGGTTT CGTCATGTTG GCCAGGCTGG TCTCAAACGC 360
CTGACCTCAG GTGATCCGCC CACCTTAGCC TCCAAAGTGC TGGGATTACA GCTGTGAGCC 420
ACTGCGCCCG GCCACAAGTG GGATTGTTAA AGGATGTGGC ATCCGATATA TTTGGCAGCA 480
CAATCGCACA GACGTGTCTC CAAGGAGGTT GGGGACAGAG AGAAAAGAGG AACAAGGAGC 540
AAGACGCAGG TTTAGGATGA TGGCATGTAG CTCAGAGGAA GGTGTGCTGG AGGCTGTTTC 600
AGTTCTGCTC CTAACCTGGG GGTGGGGGGA ACCCTGAACT AGCTGACTTC AGAGGTCCCC 660
TGCAAAGGTT TGGGACACTG GGAAGCCCAC TTCTCAGCTG GAGCTCATAT TGTTTAGGGG 720
ATAAGAAGGG AGGCCCTGAA GTCAGAGTGC CTGGCTGGGC TTCTGGCTCC GTCATTCACT 780
GGCCACGTGA CCATGTGCAA ATTCTCTGTG CTGGATGATG TTAATGTCAT AGATATTATA 840
GTAGCTGTTG TACAGGGCTG GTGTGCTGTT TAAATGAGTT CATGTAAGAG TTATGCAGTG 900
TCTTGTCCCA GAGCTTGGCA CTGTAGTAAG AACCCACTAA ATTTTAGCTC TTAGTATTAT 960
TGTTGTTTAT TTAATAAGTA ACTCCACATG GGGGCAGAGT AGCATATTGC ATGTGAAATG 1020
GGCTTGTTTC CACCTCTTGT TCTGCTATTA CCTTGTTCCA TGCCCAGCCC TGGACTCCTG 1080
AGATGGAATG GTCAGTACCT TGCCTCAAAG CACCTTTAAA CCACTAGAGC GATGACAAGG 1140
AGGTCACAGA CCCAAAGATC CCACAGCTGT ACAGGTCTGA TGGGCAGCCC TGCTGCCTTT 1200
AGGCAGGAGA CCCCAAGGGA GGGAGGGCTA GTCCAGTGGG CCAGGGAAAG GGAGCCAGGT 1260
GCTGTCAGGG 1270
|
