Variant report

Variant rs35431149
Chromosome Location chr1:192695876-192695877
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192692200-192696000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr1:192694200-192696000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:192694200-192696000 Weak transcription HMEC breast
4 chr1:192694200-192697400 Weak transcription Fetal Lung lung
5 chr1:192694400-192696000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:192694400-192698800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:192694600-192699000 Weak transcription Aorta Aorta
8 chr1:192695200-192697000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:192695800-192696000 Enhancers NHEK skin
10 chr1:192695800-192696200 Enhancers Fetal Intestine Large intestine

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