Variant report

Variant rs10775538
Chromosome Location chr19:43493817-43493818
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43490800-43494600 Enhancers NHEK skin
2 chr19:43492200-43495200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr19:43492400-43495800 Weak transcription Placenta Placenta
4 chr19:43492400-43496200 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr19:43493000-43494400 Enhancers HMEC breast
6 chr19:43493200-43494600 Enhancers NHLF lung
7 chr19:43493200-43494800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr19:43493400-43494600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr19:43493400-43496000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr19:43493800-43495400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr19:43493800-43495400 Weak transcription NHDF-Ad bronchial

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