Variant report

Variant rs2186176
Chromosome Location chr10:5095358-5095359
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5091000-5097000 Weak transcription Stomach Mucosa stomach
2 chr10:5091200-5095400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr10:5092400-5098600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr10:5095200-5096000 Enhancers Esophagus oesophagus

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