Variant report

Variant rs555406361
Chromosome Location chr9:18385793-18385794
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18379600-18392400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:18381000-18390200 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr9:18382800-18386000 Weak transcription Aorta Aorta
4 chr9:18383200-18386800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr9:18383400-18385800 Enhancers NHDF-Ad bronchial
6 chr9:18384800-18386000 Enhancers Osteobl bone
7 chr9:18384800-18386400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr9:18384800-18386600 Enhancers Colon Smooth Muscle Colon
9 chr9:18384800-18386800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr9:18385000-18386000 Enhancers Muscle Satellite Cultured Cells --
11 chr9:18385000-18386600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:18385200-18386000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr9:18385200-18386400 Enhancers HSMM muscle
14 chr9:18385400-18390400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr9:18385600-18386200 Enhancers HUVEC blood vessel

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