Variant report

Variant rs34680791
Chromosome Location chr19:43710104-43710105
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43709400-43710800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr19:43709600-43710200 Enhancers NHEK skin
3 chr19:43709600-43710200 Enhancers Osteobl bone
4 chr19:43709600-43710400 Enhancers Muscle Satellite Cultured Cells --
5 chr19:43709600-43710400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr19:43709600-43712000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr19:43709800-43710200 Flanking Active TSS IMR90 fetal lung fibroblasts Cell Line lung
8 chr19:43709800-43710200 Flanking Active TSS NHLF lung
9 chr19:43709800-43710600 Enhancers NHDF-Ad bronchial
10 chr19:43709800-43711200 Enhancers Placenta Placenta
11 chr19:43710000-43710200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
12 chr19:43710000-43710200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr19:43710000-43710200 Enhancers HMEC breast
14 chr19:43710000-43710400 Enhancers A549 lung
15 chr19:43710000-43711000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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