Variant report

Variant rs6432981
Chromosome Location chr2:168037882-168037883
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168034400-168038600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:168036400-168039000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr2:168037200-168038000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:168037200-168038800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr2:168037200-168039000 Enhancers NHEK skin
6 chr2:168037200-168039200 Enhancers HMEC breast
7 chr2:168037200-168039200 Enhancers NHLF lung
8 chr2:168037400-168038400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:168037400-168038400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:168037400-168038400 Enhancers NHDF-Ad bronchial
11 chr2:168037400-168038600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:168037400-168038800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr2:168037400-168038800 Enhancers HSMM muscle
14 chr2:168037400-168038800 Enhancers NH-A brain
15 chr2:168037400-168038800 Enhancers Osteobl bone
16 chr2:168037600-168039200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr2:168037800-168039000 Enhancers Muscle Satellite Cultured Cells --
18 chr2:168037800-168043800 Weak transcription Gastric stomach

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