Variant report

Variant rs6691292
Chromosome Location chr1:209704890-209704891
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209699000-209706000 Enhancers Muscle Satellite Cultured Cells --
2 chr1:209700200-209707000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:209700600-209705400 Enhancers HMEC breast
4 chr1:209701600-209710600 Weak transcription NHEK skin
5 chr1:209701800-209705800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:209701800-209708600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:209702200-209705600 Enhancers Pancreatic Islets Pancreatic Islet
8 chr1:209702800-209707200 Weak transcription Fetal Kidney kidney
9 chr1:209704000-209705000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:209704000-209705200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:209704600-209705200 Enhancers Stomach Mucosa stomach
12 chr1:209704600-209705400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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