| Tag | Content |
|---|
EnhancerAtlas ID | HS139-10053 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:72361560-72362670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr11:72361803-72361814 | GACAGCTGCAG | + | 6.62 | | NR2C2 | MA0504.1 | chr11:72361896-72361911 | TGACCCCTGACCCCA | - | 6.67 | | Tcf12 | MA0521.1 | chr11:72361803-72361814 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTCATCCCC CCGTGCCCCA CCTCACCGCA GATAAAGGTC CCAATCCTTC CCCAATCTCC 60
TCCCCTTAGT GGCACCTCCT ACCGTCCAGG CTGCAGAACC TGGAGGGGCT GCTCTGACTC 120
CAGCCCTAGG AGTCCCATGG AGATGCCTCC TCCTGATCCT GGTAGCAGGC TGGGTAGGGG 180
ACGAAGGAGG CAGGCTGGTC CTCTGCCAAA GGCAGCCACC CAGAGCCCTG CCCTGTACCA 240
CCAGACAGCT GCAGCCCTGA GGCTGCCCGG CTTTCCTCCA CCTGCTATTC CTGGGCTGGC 300
CCCACTCCAG GGGTGCCTCA GGTTAGAGTC AGTCCCTGAC CCCTGACCCC AGTCCCCACT 360
ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC ATACACAAAG 420
GCTACTAAGA GCTGAGCCCA TCAGAGATAC CAAGGCAAGA AGGTCTAAGC AACAGGGACC 480
AAGGCCCCAT ACTCTGAACA CTCCCTGCTA ACTCAGAAAC CATCACACAG GGAGGCCCCA 540
GTCTATGGCT TCAAGGCTCC AAGAACTCCC AGAGCTTCAT GTTCTTAGAA AATCAAAGCT 600
TCTGTTATAA CACCCCATCA TTCAAAAAGT CTGTTTTTCT TACATTCTGT GAATGCGAGA 660
ACCTGGGGTC TTGAGAATGT AGAAGCCCAA GATTCTAACA TTCTAATGTC CTGACTGCCT 720
GAGATGCCTG ATTGCAGGAC TCTAAGACTC CAGCACCTGG TTTCTATGCC CCTGAGAGCC 780
TAATGGTCAG TGGGCTTGAG TCTCTGTGAT GCCAGGTAAA GGGGAGGGCA CAGCAGCAAG 840
CACCTGTGTC TGCCTGCAGT TGGGGATACC AAGGACTGGG ATTGGGAGAG CCCAAGGAAA 900
TGAACACCCA CTCCCAAGGG GTGTCAAGGG AGTGATGGGT GTCCTGGAAG GGGCACGCAG 960
GGAGAGGCCA GGGTCTGGGG GGGTGACTCG GTCTAACCAC CATCTCCAAC TCTCCAGCTG 1020
TGTCACCTTA GACAAGTGCC TCCTGGAGAC CCCGTTTTCT CACTTCTAAA CTGGGGATCA 1080
ACTGGCCTTC CTTGAAAGGT GGCTGTGAAT 1110
|
