Variant report

Variant rs17060966
Chromosome Location chr6:132379237-132379238
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132375000-132384800 Weak transcription Pancreas Pancrea
2 chr6:132376200-132379400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr6:132376200-132379400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr6:132376200-132379400 Weak transcription Osteobl bone
5 chr6:132376200-132380600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr6:132376600-132380200 Weak transcription NHLF lung
7 chr6:132376600-132384400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr6:132377400-132379800 Weak transcription Primary hematopoietic stem cells blood
9 chr6:132378600-132379400 Weak transcription NHDF-Ad bronchial
10 chr6:132378600-132379600 Weak transcription Muscle Satellite Cultured Cells --
11 chr6:132378600-132381800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr6:132379200-132380400 Enhancers Colon Smooth Muscle Colon
13 chr6:132379200-132381800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:132379200-132385600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr6:132379200-132386200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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