Variant report

Variant rs35555343
Chromosome Location chr1:192696742-192696743
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192694200-192697400 Weak transcription Fetal Lung lung
2 chr1:192694400-192698800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr1:192694600-192699000 Weak transcription Aorta Aorta
4 chr1:192695200-192697000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:192696000-192696800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr1:192696000-192696800 Enhancers HMEC breast
7 chr1:192696200-192697200 Weak transcription Fetal Intestine Large intestine
8 chr1:192696400-192696800 Enhancers NHEK skin
9 chr1:192696400-192699000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:192696600-192697800 Weak transcription Breast Myoepithelial Primary Cells Breast

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