Variant report

Variant rs368598950
Chromosome Location chr9:18383441-18383442
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18379600-18384000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr9:18379600-18392400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:18379800-18385200 Weak transcription HSMM muscle
4 chr9:18380200-18385000 Weak transcription Muscle Satellite Cultured Cells --
5 chr9:18380400-18385000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:18381000-18390200 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr9:18382800-18384800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr9:18382800-18384800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr9:18382800-18384800 Weak transcription Colon Smooth Muscle Colon
10 chr9:18382800-18386000 Weak transcription Aorta Aorta
11 chr9:18383000-18384800 Weak transcription Osteobl bone
12 chr9:18383200-18384800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr9:18383200-18385200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr9:18383200-18386800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:18383400-18385800 Enhancers NHDF-Ad bronchial

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