Variant report

Variant rs59230671
Chromosome Location chr13:110607930-110607931
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110602000-110613600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr13:110602400-110608200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr13:110606800-110609000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr13:110607600-110608600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr13:110607600-110608600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr13:110607600-110608800 Enhancers Adipose Nuclei Adipose
7 chr13:110607600-110609000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr13:110607600-110609000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr13:110607800-110608600 Enhancers Fetal Muscle Leg muscle
10 chr13:110607800-110608600 Enhancers Lung lung

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