Variant report

Variant rs1385434
Chromosome Location chr2:151897738-151897739
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:151890600-151899600 Weak transcription Osteobl bone
2 chr2:151891400-151906400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr2:151895400-151898000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr2:151895400-151900000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr2:151896000-151898200 Enhancers Fetal Lung lung
6 chr2:151896000-151901000 Enhancers HMEC breast
7 chr2:151896600-151897800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:151897000-151905800 Weak transcription NHLF lung
9 chr2:151897000-151906000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr2:151897000-151906000 Weak transcription NHDF-Ad bronchial
11 chr2:151897400-151899000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:151897600-151899000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:151897600-151899200 Weak transcription NHEK skin

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