Variant report

Variant rs16919263
Chromosome Location chr8:54442157-54442158
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:54440200-54443400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:54441200-54442600 Enhancers HMEC breast
3 chr8:54441400-54442600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr8:54441800-54442200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr8:54441800-54442200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:54441800-54442200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr8:54441800-54442200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:54441800-54442200 Enhancers Fetal Muscle Trunk muscle
9 chr8:54441800-54442200 Enhancers Ovary ovary
10 chr8:54441800-54442200 Flanking Active TSS NHEK skin
11 chr8:54441800-54442400 Enhancers Esophagus oesophagus
12 chr8:54441800-54442800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr8:54442000-54442200 Flanking Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr8:54442000-54442200 Active TSS Breast Myoepithelial Primary Cells Breast
15 chr8:54442000-54442600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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