Variant report

Variant rs41286162
Chromosome Location chr6:132618547-132618548
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132611000-132625600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr6:132612600-132626400 Weak transcription Fetal Stomach stomach
3 chr6:132614400-132619000 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr6:132615800-132635400 Weak transcription Fetal Lung lung
5 chr6:132616200-132620400 Weak transcription Esophagus oesophagus
6 chr6:132616200-132625200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr6:132616600-132625200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr6:132617000-132618800 Strong transcription NHDF-Ad bronchial
9 chr6:132617200-132618600 Strong transcription Osteobl bone
10 chr6:132617200-132627600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr6:132617600-132619000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr6:132617600-132619200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:132617600-132626200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr6:132618000-132619000 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr6:132618200-132619000 Enhancers Brain Hippocampus Middle brain
16 chr6:132618400-132618600 Genic enhancers Cortex derived primary cultured neurospheres brain
17 chr6:132618400-132631600 Weak transcription Fetal Kidney kidney

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