| Tag | Content |
|---|
EnhancerAtlas ID | HS139-50782 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr7:72857160-72858310 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr7:72857681-72857691 | GGGGCGGGGC | - | 6.02 | | SCRT1 | MA0743.1 | chr7:72858225-72858240 | TCCCACCTGTTGCCT | - | 6.29 | | SP1 | MA0079.4 | chr7:72857679-72857694 | AAGGGGCGGGGCCTC | - | 6.18 | | SP4 | MA0685.1 | chr7:72857677-72857694 | AAAAGGGGCGGGGCCTC | - | 6.79 | | ZNF263 | MA0528.1 | chr7:72858198-72858219 | TAAGAAGGAGGAGGGGGGAGG | + | 6.53 |
|
| | 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 |
| GH07I073441 | chr7 | 72856010 | 72859944 |
|
Enhancer Sequence | GGCAGGAAAG AAAGAACAAT GTTATTACAG ATTCAAGACA GGAGGAAGAA TGGACAGGGC 60
AGAAAATAAG TGTATCTGCT CAAAAAAGGA AGAGAGTTCA ACTATTTCCT TGGCGCAGAG 120
GTGCTGAAAC CTTCTGATAT TCAAGTCAGG GAGCACCCTC GGCCCAGGTG GCAGGCATCT 180
TCCCAGTAGT CCACTCACTC GCCTCCCCCG GGGCCACGGC AATCAAAGCA GCAAAGAGCA 240
GGCAGCGGGG GCCGCCTTTA CCAGCAGTCC TGCTGGAGGT CGGCTGAAGG GGGCTACTGT 300
CAACAGGACA CTAGCTCTCA GAGAACAGGT GGACCTGGGG TTACAGTGAC ACCATGGAAG 360
GGCATCAACA AGCCACTGCA GAAAGCAAAA CATGCTATCT GGGCCAACAG CAGCCAATTC 420
TGTGGGGGTG GGGTGCCTCT GGTAAGAAAA GCAAGAGGTC CAATTCCCTT CCTGGGCTCT 480
TCCACCGTAG ACATGTGAGG GTTAAGTGGC TAAAGAGAAA AGGGGCGGGG CCTCCATTCC 540
AGGTAGCCAT AACAAAAGCT GTGATTCACA GCAGAGGCCA CAGAGCCCAA GGCTGTGGCA 600
AACCGAGCAT CTTCTAATGC CTTATGATCT CCCAAATGGC CTGCCTTAAG CCCCTAACTC 660
CAATTTGATC TGTCAAAACA AGCACCTTTT CAAGAGTTTC TTTTTTGTTC TTTAAAGCTC 720
AAGTGAGATC TAAAAACTAC TAAAATTACA TTGGTTAAGG AGCAGAGGGG AGGGTAATGT 780
CCCTCCCATA ACAACTGTCG ACTCAACAGT AAGTGAGGCT CCAGCATTGC TGACATTCCC 840
ACAATGAAGA CCCAGCCCCT CTGAGCCCAC TGGAGACACA TGGATACTAT TTTTAAATCC 900
TTAATAAGTT GCAGGCTGCC CGCTAACTAG TTTGCAGGCT ACAGCAGGGG AATGCCGGAC 960
ATAGCTGTTC CTGGAGGCCT TGCTGCTTCT GTCTGCGTAC AGGCTCACCC ATCTGCCTCC 1020
CCAGCCTCCC AAGTTTGGTA AGAAGGAGGA GGGGGGAGGC TCCCCTCCCA CCTGTTGCCT 1080
GATGAATTCC TAATTGCTGG GGTAGGGAAT AAGAAACAGA AAGGTTAGAG AAGGGATGAT 1140
AAATAATTCT 1150
|
