| Tag | Content |
|---|
EnhancerAtlas ID | HS060-07182 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:126354610-126355830 |
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 | TGATTTAATT AATGTAGGTG TGCTTTCCCC CTCTTCAGAC CCTCCCCGCC TCCACTTAGG 60
TCTATATTAA GAAGATGTGG GGCAAGATGC AAATGGGATT TTTTTTTTTT TTTTTCTGAG 120
ACGGAGTCTC GCTCTTGTCA CCCAGGCTGG AGTGCAATGG CACAATGTAG GCTCACTGCA 180
GCCTCCGCCT CCCAGGTTCA AGCGATTCTC CTGCCTCAGC CTTTTAAATA GCTGGGATTA 240
CAGGCACCTG CCACCACGCC TGGCTGATAT TTTTTGGTAC TTTTGGTGGA GACGGGGTTT 300
CGTCATGTTG GCCAGGCTGG TCTCAAACGC CTGACCTCAG GTGATCCGCC CACCTTAGCC 360
TCCAAAGTGC TGGGATTACA GCTGTGAGCC ACTGCGCCCG GCCACAAGTG GGATTGTTAA 420
AGGATGTGGC ATCCGATATA TTTGGCAGCA CAATCGCACA GACGTGTCTC CAAGGAGGTT 480
GGGGACAGAG AGAAAAGAGG AACAAGGAGC AAGACGCAGG TTTAGGATGA TGGCATGTAG 540
CTCAGAGGAA GGTGTGCTGG AGGCTGTTTC AGTTCTGCTC CTAACCTGGG GGTGGGGGGA 600
ACCCTGAACT AGCTGACTTC AGAGGTCCCC TGCAAAGGTT TGGGACACTG GGAAGCCCAC 660
TTCTCAGCTG GAGCTCATAT TGTTTAGGGG ATAAGAAGGG AGGCCCTGAA GTCAGAGTGC 720
CTGGCTGGGC TTCTGGCTCC GTCATTCACT GGCCACGTGA CCATGTGCAA ATTCTCTGTG 780
CTGGATGATG TTAATGTCAT AGATATTATA GTAGCTGTTG TACAGGGCTG GTGTGCTGTT 840
TAAATGAGTT CATGTAAGAG TTATGCAGTG TCTTGTCCCA GAGCTTGGCA CTGTAGTAAG 900
AACCCACTAA ATTTTAGCTC TTAGTATTAT TGTTGTTTAT TTAATAAGTA ACTCCACATG 960
GGGGCAGAGT AGCATATTGC ATGTGAAATG GGCTTGTTTC CACCTCTTGT TCTGCTATTA 1020
CCTTGTTCCA TGCCCAGCCC TGGACTCCTG AGATGGAATG GTCAGTACCT TGCCTCAAAG 1080
CACCTTTAAA CCACTAGAGC GATGACAAGG AGGTCACAGA CCCAAAGATC CCACAGCTGT 1140
ACAGGTCTGA TGGGCAGCCC TGCTGCCTTT AGGCAGGAGA CCCCAAGGGA GGGAGGGCTA 1200
GTCCAGTGGG CCAGGGAAAG 1220
|
