Variant report

Variant rs140042176
Chromosome Location chr7:110839095-110839096
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:110837400-110840000 Enhancers Muscle Satellite Cultured Cells --
2 chr7:110837600-110839200 Enhancers HMEC breast
3 chr7:110837600-110839200 Enhancers NH-A brain
4 chr7:110837600-110839200 Enhancers NHEK skin
5 chr7:110837600-110839200 Enhancers NHLF lung
6 chr7:110837600-110839400 Enhancers HSMM muscle
7 chr7:110837600-110839800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr7:110837600-110840000 Enhancers Osteobl bone
9 chr7:110838200-110846600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:110838400-110839200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr7:110838400-110839200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr7:110838400-110839600 Enhancers NHDF-Ad bronchial
13 chr7:110838400-110840200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr7:110838800-110864000 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr7:110839000-110839200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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