Variant report

Variant rs17707596
Chromosome Location chr2:184092114-184092115
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:184072600-184094000 Weak transcription HSMM muscle
2 chr2:184085200-184097000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:184087600-184094000 Weak transcription HSMMtube muscle
4 chr2:184089400-184092400 Enhancers Fetal Brain Male brain
5 chr2:184089400-184093000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr2:184089600-184093000 Enhancers Skeletal Muscle Female skeletal muscle
7 chr2:184090200-184094000 Weak transcription Osteobl bone
8 chr2:184090200-184095800 Weak transcription Brain Hippocampus Middle brain
9 chr2:184090400-184094000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:184091600-184092200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr2:184091600-184092800 Enhancers Skeletal Muscle Male skeletal muscle
12 chr2:184091600-184093000 Enhancers Fetal Muscle Leg muscle
13 chr2:184091600-184093000 Enhancers Psoas Muscle Psoas
14 chr2:184091800-184092400 Enhancers Fetal Heart heart
15 chr2:184092000-184092200 Enhancers Fetal Brain Female brain

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