Variant report

Variant rs13141904
Chromosome Location chr4:21771110-21771111
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:21766600-21780200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr4:21769400-21780400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr4:21770000-21771400 Enhancers NHEK skin
4 chr4:21770000-21771600 Enhancers Muscle Satellite Cultured Cells --
5 chr4:21770000-21771600 Enhancers HMEC breast
6 chr4:21770000-21771600 Enhancers Osteobl bone
7 chr4:21770200-21771600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr4:21770400-21771200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr4:21770400-21771400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr4:21770600-21771200 Enhancers Hela-S3 cervix
11 chr4:21770600-21771600 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr4:21770600-21771800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr4:21770600-21771800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr4:21770800-21771400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr4:21771000-21771600 Enhancers HUVEC blood vessel
16 chr4:21771000-21771800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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