Variant report

Variant rs12472298
Chromosome Location chr2:189830499-189830500
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:189814000-189830800 Weak transcription Pancreas Pancrea
2 chr2:189828400-189838400 Weak transcription Fetal Kidney kidney
3 chr2:189828600-189830600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr2:189829000-189830800 Weak transcription NHDF-Ad bronchial
5 chr2:189829000-189833600 Weak transcription Fetal Stomach stomach
6 chr2:189829200-189833600 Weak transcription NHLF lung
7 chr2:189829600-189830600 Weak transcription Adipose Nuclei Adipose
8 chr2:189829800-189830800 Enhancers Fetal Lung lung
9 chr2:189830200-189830800 Weak transcription Colon Smooth Muscle Colon
10 chr2:189830400-189830600 Enhancers Aorta Aorta
11 chr2:189830400-189830600 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr2:189830400-189831200 Enhancers Ovary ovary
13 chr2:189830400-189832000 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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