Variant report

Variant rs9260960
Chromosome Location chr6:29960958-29960959
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29945600-29966400 Weak transcription Pancreas Pancrea
2 chr6:29960000-29961400 Enhancers Fetal Intestine Large intestine
3 chr6:29960000-29961600 Enhancers NHDF-Ad bronchial
4 chr6:29960200-29961400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr6:29960400-29961000 Enhancers NHEK skin
6 chr6:29960400-29961200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:29960400-29961200 Enhancers HMEC breast
8 chr6:29960400-29961400 Enhancers Fetal Intestine Small intestine
9 chr6:29960600-29961000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr6:29960600-29961200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr6:29960800-29961200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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