Variant report

Variant rs1911546
Chromosome Location chr1:215649097-215649098
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215646800-215650000 Enhancers Placenta Amnion Placenta Amnion
2 chr1:215647000-215650400 Enhancers HSMM muscle
3 chr1:215647200-215649400 Enhancers NHDF-Ad bronchial
4 chr1:215647200-215650000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr1:215647600-215649800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:215647600-215650200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:215647800-215651000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:215648200-215650000 Enhancers NHLF lung
9 chr1:215648200-215650200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:215648400-215650000 Enhancers NH-A brain
11 chr1:215648400-215650200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:215648400-215650400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:215648400-215650400 Enhancers HMEC breast
14 chr1:215648400-215650400 Enhancers NHEK skin
15 chr1:215648400-215650600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr1:215648600-215650000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr1:215648800-215650600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
18 chr1:215648800-215663200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr1:215649000-215649200 Flanking Active TSS HSMMtube muscle
20 chr1:215649000-215649200 Flanking Active TSS Osteobl bone
21 chr1:215649000-215649800 Flanking Active TSS Muscle Satellite Cultured Cells --

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