Variant report

Variant rs533449390
Chromosome Location chr4:187852205-187852206
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187837200-187863800 Weak transcription Right Atrium heart
2 chr4:187840000-187853400 Weak transcription Fetal Kidney kidney
3 chr4:187842000-187852400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr4:187846400-187853400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr4:187851400-187854000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr4:187851800-187853000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr4:187851800-187853400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr4:187851800-187855800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:187851800-187857800 Enhancers Osteobl bone
10 chr4:187852000-187853000 Enhancers NHDF-Ad bronchial
11 chr4:187852000-187854200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:187852000-187854400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr4:187852000-187855000 Enhancers HSMM muscle
14 chr4:187852200-187853000 Enhancers Muscle Satellite Cultured Cells --
15 chr4:187852200-187853800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr4:187852200-187854400 Enhancers HMEC breast
17 chr4:187852200-187854600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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