Variant report

Variant rs12567579
Chromosome Location chr1:172891322-172891323
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172888000-172897200 Weak transcription Colon Smooth Muscle Colon
2 chr1:172888200-172895600 Weak transcription Osteobl bone
3 chr1:172888400-172897000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:172888800-172897400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr1:172889400-172895600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:172889400-172897000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:172889400-172897000 Weak transcription HMEC breast
8 chr1:172889400-172897200 Weak transcription HUVEC blood vessel
9 chr1:172889400-172897200 Weak transcription NHDF-Ad bronchial
10 chr1:172889600-172896200 Weak transcription HSMM muscle
11 chr1:172890400-172896600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:172890400-172897200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr1:172890800-172897400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:172891000-172895800 Weak transcription Muscle Satellite Cultured Cells --
15 chr1:172891000-172896600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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