Variant report

Variant rs13135188
Chromosome Location chr4:21770519-21770520
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:21766000-21771000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr4:21766600-21780200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:21769400-21780400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr4:21770000-21771000 Enhancers NH-A brain
5 chr4:21770000-21771400 Enhancers NHEK skin
6 chr4:21770000-21771600 Enhancers Muscle Satellite Cultured Cells --
7 chr4:21770000-21771600 Enhancers HMEC breast
8 chr4:21770000-21771600 Enhancers Osteobl bone
9 chr4:21770200-21770600 Enhancers HUVEC blood vessel
10 chr4:21770200-21771600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr4:21770400-21771200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr4:21770400-21771400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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