Variant report

Variant rs10798249
Chromosome Location chr1:172972931-172972932
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172960600-172974000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:172968200-172973600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:172972000-172973000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:172972000-172973000 Enhancers HMEC breast
5 chr1:172972000-172973200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:172972000-172973200 Enhancers Muscle Satellite Cultured Cells --
7 chr1:172972200-172973200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:172972800-172973000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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