Variant report

Variant rs73644246
Chromosome Location chr9:18564404-18564405
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18546200-18564600 Weak transcription NH-A brain
2 chr9:18546200-18574000 Weak transcription Fetal Heart heart
3 chr9:18555800-18564800 Weak transcription HUVEC blood vessel
4 chr9:18563600-18565800 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr9:18563600-18569400 Weak transcription Rectal Smooth Muscle rectum
6 chr9:18564000-18564600 Genic enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:18564200-18565600 Genic enhancers HSMM muscle
8 chr9:18564200-18566400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:18564200-18567000 Enhancers NHDF-Ad bronchial
10 chr9:18564200-18567000 Enhancers Osteobl bone
11 chr9:18564400-18564600 Enhancers HSMMtube muscle
12 chr9:18564400-18565600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:18564400-18565600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
14 chr9:18564400-18566200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr9:18564400-18566400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr9:18564400-18566400 Enhancers Muscle Satellite Cultured Cells --
17 chr9:18564400-18566400 Weak transcription Fetal Stomach stomach
18 chr9:18564400-18566800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr9:18564400-18569000 Weak transcription Aorta Aorta
20 chr9:18564400-18591800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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