| Tag | Content |
|---|
EnhancerAtlas ID | HS139-10865 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:118041570-118042910 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:118042509-118042528 | GCGTGCCCTCTAGTGGTCA | - | 7.07 | | KLF5 | MA0599.1 | chr11:118041763-118041773 | GCCCCGCCCC | + | 6.02 | | Sox6 | MA0515.1 | chr11:118042617-118042627 | CCATTGTTTT | + | 6.02 | | ZNF263 | MA0528.1 | chr11:118042374-118042395 | GGGGGAGGGCAGGGTAGAGAG | + | 6.01 |
|
| | 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 |
| GH11I118171 | chr11 | 118042057 | 118042766 |
|
Enhancer Sequence | GGGGAGCCTC TGGCCTGGCC TGAGGGCACC TTGGAGACTG CCCCACTCCA ACCAGTCCGT 60
AGGAATTGGC GAACAGCCCA GGCCTGCAGG GCTCCTATTT TTCAAACTTT TTTTTTTTCT 120
TCACAAAGCC GTAGAAGCAG CCGCCCTGCA GCCTGCAGGG AAATCAACAT CTGCCTGGAG 180
CACCCTTCTG CCAGCCCCGC CCCTGGCCCG AGTGACCAGG GCAAATGGCA GGACTTAAGA 240
ACCAGAGATT CTCTGAACTG GCAGCAGCCC TGGATGGAGG GGTAGGCATG GGGACCTCAT 300
CTGTTCTCCA AGCTGGGAGA CAGCTGTCAC CATCTGCGTT TTCTAGAGGA GGAGTCCAGG 360
GCCGAGGATT CCAGGTGTGA GCTTAAGTGC TCATTAGGGG AATAAGGACT GGGGAGGCTG 420
AGTGGGCCCC TGTCAGGAAG AACAAAGCCC AATTCCATCT CCTGTACTTT CATCGCCGTT 480
CTGAAAGCAT CTGGCAGCGC ACCAGCCAAG GAGGAGGTGT GCAGAAAATG CCAACAGCAT 540
CTTCATCTGC AGAGGCCCAG AGCTCTGAGG GAAGGCACTG ACAGTGCTTG TCCTGAGCTT 600
ACCTCCCATC CCAGGAATGT CCTATCCCTC TAGCTCTTCC CTTGGAAGGT CGATCATCTT 660
CCCAGGGGCT CCCCAGACCA AAAAGTCTGC GTTCTGCGAA GCCCGGCGGA CTCTGTGCGG 720
GCCTCTGCCC CCCACCAAGC CCAAGGCAGT GCTCCAGATT AGAACTTGAA CCTCACCATC 780
TCGAAGGAGC TAGCACCCTG CCGTGGGGGA GGGCAGGGTA GAGAGGAGTG CGGGGGCGCC 840
TTTTCTGGCC GGCAGGACGG GGGCAGCCGG AGAGGTGCAA TGCGGGCTCC CCCTCCCCAC 900
CCTGCAGCGG GGCCCTGCAG AAGGTACCGG GCGGAACACG CGTGCCCTCT AGTGGTCACA 960
GAGTCAAACG TCAAGTTCCA TCCTGCGGAG CGAGCATGGG ATCCGGAGCC ACAGCTGGAG 1020
CTGAGATCAG AAACCGTAGA TCTAGCCCCA TTGTTTTACC GGTGAGGAAA GGCCATGAGA 1080
GCCACACACA GAGAATAGGG ACAAGCTGAG GCCAGAATCA TGGTTCCTAG CCCCTAATCC 1140
AATATCTCCA CGTAAGCCTG TGGCCTCACC AGAATCCCAG CAGCTCTAGG GTGCTGGCCT 1200
CAGACCTCCC GCCAGTCCGG GCCCTCATTA AAGACGAGGG GACCATGGCT CAACAAGGTC 1260
AGAGCTGTGA GCAAAACTCT GGTCTCTTGA TTAACTCTCC TGCTTCGGGA AAGCACCCGA 1320
ATGCATGGCC AAGGCCACAG 1340
|
