Variant report

Variant rs9321320
Chromosome Location chr6:132379813-132379814
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132375000-132384800 Weak transcription Pancreas Pancrea
2 chr6:132376200-132380600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr6:132376600-132380200 Weak transcription NHLF lung
4 chr6:132376600-132384400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:132378600-132381800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:132379200-132380400 Enhancers Colon Smooth Muscle Colon
7 chr6:132379200-132381800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr6:132379200-132385600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr6:132379200-132386200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr6:132379400-132380400 Enhancers Ovary ovary
11 chr6:132379400-132380800 Enhancers Osteobl bone
12 chr6:132379400-132381000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:132379400-132383400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr6:132379400-132385600 Enhancers NHDF-Ad bronchial
15 chr6:132379600-132386200 Enhancers Muscle Satellite Cultured Cells --
16 chr6:132379800-132380000 Enhancers Primary hematopoietic stem cells blood
17 chr6:132379800-132383600 Enhancers Brain Germinal Matrix brain
18 chr6:132379800-132384400 Weak transcription Fetal Heart heart

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