Variant report

Variant rs59196614
Chromosome Location chr9:97654752-97654753
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:97633400-97671800 Weak transcription Esophagus oesophagus
2 chr9:97638600-97661800 Weak transcription Fetal Intestine Small intestine
3 chr9:97648000-97657400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:97648400-97656400 Weak transcription NH-A brain
5 chr9:97648400-97657400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:97648600-97654800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr9:97648600-97656000 Weak transcription Liver Liver
8 chr9:97650400-97655800 Weak transcription Stomach Mucosa stomach
9 chr9:97650600-97656000 Weak transcription NHLF lung
10 chr9:97651000-97655400 Weak transcription Hela-S3 cervix
11 chr9:97653400-97662400 Weak transcription Fetal Brain Male brain
12 chr9:97653600-97656200 Weak transcription HSMM muscle
13 chr9:97653800-97654800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr9:97654200-97655000 Weak transcription A549 lung
15 chr9:97654400-97654800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr9:97654400-97655200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr9:97654400-97656000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr9:97654600-97655000 Enhancers Osteobl bone
19 chr9:97654600-97655800 Enhancers Pancreas Pancrea
20 chr9:97654600-97656200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
21 chr9:97654600-97656800 Enhancers NHEK skin
22 chr9:97654600-97658800 Enhancers Muscle Satellite Cultured Cells --

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