Variant report

Variant rs530133215
Chromosome Location chr9:18631927-18631928
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18606600-18632200 Weak transcription NHLF lung
2 chr9:18621600-18632000 Weak transcription HSMMtube muscle
3 chr9:18621800-18632400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr9:18623000-18633200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:18623200-18632600 Weak transcription Fetal Stomach stomach
6 chr9:18625200-18632000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:18627200-18632000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr9:18628000-18632000 Weak transcription NH-A brain
9 chr9:18628400-18632000 Weak transcription NHDF-Ad bronchial
10 chr9:18629200-18632000 Weak transcription Right Atrium heart
11 chr9:18629200-18632600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr9:18629600-18632800 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr9:18630000-18632600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:18630000-18632800 Enhancers Osteobl bone
15 chr9:18630400-18632600 Weak transcription Fetal Heart heart
16 chr9:18631000-18632000 Weak transcription Brain Anterior Caudate brain
17 chr9:18631000-18666400 Weak transcription Aorta Aorta
18 chr9:18631600-18632600 Enhancers Muscle Satellite Cultured Cells --
19 chr9:18631800-18633000 Enhancers HUVEC blood vessel
20 chr9:18631800-18634200 Enhancers HSMM muscle

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