Variant report

Variant rs2085583
Chromosome Location chr3:50888677-50888678
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:50886000-50899800 Weak transcription Brain Inferior Temporal Lobe brain
2 chr3:50888200-50889000 Enhancers HUES48 Cell Line embryonic stem cell
3 chr3:50888200-50889200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr3:50888200-50889200 Enhancers NHEK skin
5 chr3:50888200-50889400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr3:50888200-50889400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr3:50888200-50889400 Enhancers HMEC breast
8 chr3:50888400-50889000 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr3:50888400-50889200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr3:50888400-50889200 ZNF genes & repeats Esophagus oesophagus
11 chr3:50888600-50888800 Enhancers H9 Cell Line embryonic stem cell
12 chr3:50888600-50888800 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr3:50888600-50889000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr3:50888600-50889200 Enhancers H1 Cell Line embryonic stem cell
15 chr3:50888600-50889200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
16 chr3:50888600-50889200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
17 chr3:50888600-50889600 Enhancers Right Ventricle heart

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