Variant report

Variant rs10416723
Chromosome Location chr19:43438750-43438751
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43433800-43439600 Enhancers HMEC breast
2 chr19:43434200-43440200 Enhancers NHDF-Ad bronchial
3 chr19:43434800-43439800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr19:43435400-43439600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr19:43435800-43439200 Enhancers Osteobl bone
6 chr19:43435800-43439400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr19:43435800-43439600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr19:43435800-43439800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr19:43436000-43439000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr19:43436000-43439600 Enhancers Muscle Satellite Cultured Cells --
11 chr19:43436400-43439000 Enhancers NH-A brain
12 chr19:43437400-43439400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr19:43437400-43439800 Enhancers NHLF lung
14 chr19:43437600-43440200 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr19:43438000-43439600 Enhancers Fetal Muscle Leg muscle
16 chr19:43438600-43439400 Weak transcription NHEK skin
17 chr19:43438600-43441600 Active TSS Placenta Placenta

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