Variant report

Variant rs35665436
Chromosome Location chr9:18634709-18634710
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18631000-18666400 Weak transcription Aorta Aorta
2 chr9:18632800-18640400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:18633000-18637200 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr9:18633000-18642800 Weak transcription Fetal Heart heart
5 chr9:18633400-18636600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr9:18633400-18636600 Weak transcription HSMMtube muscle
7 chr9:18633400-18637800 Weak transcription NHLF lung
8 chr9:18633400-18638200 Weak transcription NH-A brain
9 chr9:18633600-18635400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:18633600-18638800 Weak transcription Fetal Stomach stomach
11 chr9:18634400-18634800 Weak transcription Osteobl bone
12 chr9:18634400-18635800 Weak transcription NHDF-Ad bronchial
13 chr9:18634400-18636600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr9:18634400-18638000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr9:18634600-18635800 Weak transcription HSMM muscle
16 chr9:18634600-18636400 Weak transcription Muscle Satellite Cultured Cells --
17 chr9:18634600-18638200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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