Variant report

Variant rs58684857
Chromosome Location chr19:43439739-43439740
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43434200-43440200 Enhancers NHDF-Ad bronchial
2 chr19:43434800-43439800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr19:43435800-43439800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr19:43437400-43439800 Enhancers NHLF lung
5 chr19:43437600-43440200 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr19:43438600-43441600 Active TSS Placenta Placenta
7 chr19:43439200-43442400 Weak transcription Osteobl bone
8 chr19:43439400-43442600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr19:43439400-43443800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr19:43439600-43443600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:43439600-43443600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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