Variant report

Variant rs10267292
Chromosome Location chr7:17001008-17001009
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16988600-17009000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:16991200-17002200 Weak transcription Stomach Mucosa stomach
3 chr7:16999600-17002600 Weak transcription HepG2 liver
4 chr7:16999600-17003400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr7:16999800-17002200 Enhancers Muscle Satellite Cultured Cells --
6 chr7:16999800-17002400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:16999800-17002400 Enhancers HSMM muscle
8 chr7:16999800-17002400 Enhancers Osteobl bone
9 chr7:16999800-17002600 Enhancers NHDF-Ad bronchial
10 chr7:17000000-17001200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr7:17000400-17001200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr7:17000800-17003400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr7:17000800-17003800 Enhancers Hela-S3 cervix
14 chr7:17001000-17001400 Active TSS HSMMtube muscle
15 chr7:17001000-17002000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:17001000-17002000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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