Variant report

Variant rs2144909
Chromosome Location chr14:67325444-67325445
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67310200-67326600 Weak transcription Left Ventricle heart
2 chr14:67320400-67325800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr14:67321600-67326000 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr14:67323600-67325800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr14:67323600-67325800 Weak transcription NHEK skin
6 chr14:67323600-67326000 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr14:67323600-67327400 Weak transcription Psoas Muscle Psoas
8 chr14:67324000-67341400 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr14:67324400-67326400 Enhancers HepG2 liver
10 chr14:67324800-67325600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr14:67325000-67327400 Weak transcription Pancreas Pancrea
12 chr14:67325200-67326000 Weak transcription Liver Liver
13 chr14:67325400-67325600 ZNF genes & repeats Fetal Stomach stomach
14 chr14:67325400-67326000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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