Variant report

Variant rs4699213
Chromosome Location chr4:102289107-102289108
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:102287000-102289400 Enhancers NHDF-Ad bronchial
2 chr4:102287000-102289400 Enhancers Osteobl bone
3 chr4:102287000-102289600 Enhancers NHEK skin
4 chr4:102287200-102289200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr4:102287200-102289200 Enhancers NHLF lung
6 chr4:102287200-102289400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr4:102287200-102289400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr4:102287200-102289400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:102287200-102289800 Enhancers HMEC breast
10 chr4:102287400-102289200 Enhancers Muscle Satellite Cultured Cells --
11 chr4:102287400-102289400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:102287600-102289600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:102288200-102289200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr4:102288200-102289200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr4:102288200-102289200 Enhancers NH-A brain
16 chr4:102288800-102289200 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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