Variant report

Variant rs2107457
Chromosome Location chr19:43335513-43335514
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43321400-43337400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr19:43325200-43335600 Weak transcription NHLF lung
3 chr19:43325400-43337400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr19:43328600-43335600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr19:43334400-43335600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43334400-43338200 Enhancers HMEC breast
7 chr19:43334800-43336200 Enhancers Brain Hippocampus Middle brain
8 chr19:43334800-43336800 Enhancers Brain Angular Gyrus brain
9 chr19:43334800-43336800 Enhancers Brain Substantia Nigra brain
10 chr19:43335000-43335800 Enhancers Brain Inferior Temporal Lobe brain
11 chr19:43335000-43336000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr19:43335200-43337000 Flanking Active TSS A549 lung
13 chr19:43335400-43336000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr19:43335400-43336600 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr19:43335400-43337600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr19:43335400-43337800 Enhancers NHEK skin
17 chr19:43335400-43338200 Enhancers HSMMtube muscle

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