Variant report

Variant rs686338
Chromosome Location chr1:186206889-186206890
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:186203600-186208600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr1:186204000-186207000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:186204000-186207600 Enhancers HMEC breast
4 chr1:186204000-186207600 Enhancers NHEK skin
5 chr1:186204200-186207000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:186205200-186207000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:186205200-186207000 Enhancers Placenta Placenta
8 chr1:186205200-186208800 Enhancers NHDF-Ad bronchial
9 chr1:186205600-186207600 Enhancers NHLF lung
10 chr1:186205600-186208400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:186205800-186207200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr1:186206400-186207400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr1:186206600-186207600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr1:186206600-186208200 Weak transcription Osteobl bone
15 chr1:186206600-186208400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:186206800-186207200 Weak transcription Muscle Satellite Cultured Cells --

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