Variant report

Variant rs72994375
Chromosome Location chr1:119903379-119903380
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:119897600-119903400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:119898400-119906200 Strong transcription Liver Liver
3 chr1:119899200-119905800 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr1:119901800-119905800 Weak transcription H1 Cell Line embryonic stem cell
5 chr1:119901800-119907200 Weak transcription NHDF-Ad bronchial
6 chr1:119902000-119903800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:119902000-119907200 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr1:119902200-119907000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:119902400-119907000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:119902400-119907000 Weak transcription HMEC breast
11 chr1:119902400-119907000 Weak transcription NHEK skin
12 chr1:119902400-119907200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:119902800-119903800 Weak transcription GM12878-XiMat blood

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