| Tag | Content |
|---|
EnhancerAtlas ID | HS060-07030 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:119130610-119131310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr11:119131095-119131105 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:119131095-119131105 | GGCACGTGCC | - | 6.02 | | SPI1 | MA0080.4 | chr11:119130842-119130856 | AACTTCCTCTTTCA | - | 6.03 |
|
| | 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 |
| GH11I119257 | chr11 | 119128485 | 119131878 |
|
Enhancer Sequence | TCTATCTCAC TTACCTCCAC ACTCTTCTCA AAGGGGGAAA CTCAGTTTCA GCTTGATTAT 60
CTTGTACAAG GGCACTAGCA AATGGACCGT TCCATTCCCA GAGATGCCAA CAATCTTACA 120
CAGATTATTC ACAAATCTGT TTTCCCAAGC TACCTGCTAG TTATACTCAT GTTAGTATCT 180
TCCCACACTC AAAATACCTG AACACTGAAT GTATCCTCTT CATCAGCAAA CCAACTTCCT 240
CTTTCATGTC CCGTTACTGA GTTAGTACTG TATAATGTAG TGAGTAGTGA TGATGAGCAT 300
GGATTGATTA TTGGCTTAGC TTCTTTTTTT TTTTTTCTTT TTCTTTTCTT TTCTTTTTTT 360
TTGAGATGGA GTGTCACTCT GTCGTTCAGA CTGGATTTAG TGGTGCAATC TCGGCTCACT 420
GCAACCTCCA CCTCCTGGGT TCAATCAATT CTCCTGCCTC AGCCTCCCGA GTAGCTGCGA 480
CTACAGGCAC GTGCCATCAC GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTT 540
ACCATGTTGA CCAGGCTGGT CGGCTCAGCT TCTTTATGCC TAAATTGTCT CATCTGTAAA 600
ATGGGGATAA TATTGGAATC TGATGGGATT GTAAGTGAGA ATTAGTTAAA TAACAAAATA 660
CGTAAAGTGC CTGGTACTTA GTAAGCCCTT AAAAAACATT 700
|
