Variant report

Variant rs10167914
Chromosome Location chr2:113563361-113563362
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113560600-113563600 Enhancers HMEC breast
2 chr2:113561200-113563600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:113561400-113563600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:113561600-113563600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr2:113561800-113563600 Enhancers HepG2 liver
6 chr2:113562200-113563400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:113562200-113563400 Weak transcription K562 blood
8 chr2:113562800-113563400 Enhancers Placenta Amnion Placenta Amnion
9 chr2:113562800-113563600 Enhancers Primary B cells from peripheral blood blood
10 chr2:113562800-113563600 Enhancers Esophagus oesophagus
11 chr2:113562800-113563600 Flanking Active TSS GM12878-XiMat blood
12 chr2:113562800-113563600 Flanking Active TSS NHEK skin
13 chr2:113563000-113563400 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr2:113563000-113563600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr2:113563000-113563600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr2:113563200-113563400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
17 chr2:113563200-113563400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
18 chr2:113563200-113563600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr2:113563200-113563600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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