Variant report

Variant rs148795991
Chromosome Location chr9:72218470-72218471
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:72207800-72220200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr9:72209200-72219600 Weak transcription Gastric stomach
3 chr9:72212000-72219200 Weak transcription Liver Liver
4 chr9:72215000-72219600 Weak transcription Right Ventricle heart
5 chr9:72215000-72220200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:72215200-72219600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:72215200-72221000 Weak transcription Right Atrium heart
8 chr9:72215400-72219200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr9:72215600-72235200 Weak transcription Aorta Aorta
10 chr9:72217200-72221200 Enhancers Ovary ovary
11 chr9:72217600-72219200 Weak transcription Fetal Brain Male brain
12 chr9:72218200-72219000 Weak transcription Pancreas Pancrea
13 chr9:72218200-72219000 Weak transcription Spleen Spleen
14 chr9:72218200-72219800 Weak transcription Fetal Heart heart
15 chr9:72218200-72220400 Weak transcription Fetal Muscle Leg muscle
16 chr9:72218400-72218800 Weak transcription HUVEC blood vessel

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