Variant report

Variant rs2095100
Chromosome Location chr9:18594874-18594875
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18569800-18601000 Weak transcription NHLF lung
2 chr9:18583800-18595000 Weak transcription Fetal Stomach stomach
3 chr9:18584000-18603200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:18584800-18595600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr9:18588600-18605600 Weak transcription NH-A brain
6 chr9:18592000-18595400 Weak transcription Rectal Mucosa Donor 29 rectum
7 chr9:18592200-18595400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr9:18592200-18595400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr9:18592200-18596800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr9:18592400-18595200 Weak transcription NHDF-Ad bronchial
11 chr9:18592600-18595200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:18592600-18596600 Weak transcription Muscle Satellite Cultured Cells --
13 chr9:18592600-18605800 Weak transcription Aorta Aorta
14 chr9:18594200-18605800 Weak transcription HSMMtube muscle
15 chr9:18594800-18595200 Strong transcription Osteobl bone
16 chr9:18594800-18595400 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr9:18594800-18595400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr9:18594800-18595400 ZNF genes & repeats HSMM muscle
19 chr9:18594800-18596000 Genic enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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