Variant report

Variant rs6475576
Chromosome Location chr9:21765601-21765602
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21762600-21770200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:21764600-21767200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr9:21765400-21770400 Weak transcription NHLF lung
4 chr9:21765400-21770600 Weak transcription Muscle Satellite Cultured Cells --
5 chr9:21765400-21770600 Weak transcription NH-A brain
6 chr9:21765400-21770600 Weak transcription Osteobl bone
7 chr9:21765400-21772600 Weak transcription HSMM muscle
8 chr9:21765600-21770200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:21765600-21770400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:21765600-21770600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:21765600-21770600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr9:21765600-21770600 Weak transcription NHDF-Ad bronchial
13 chr9:21765600-21770800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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