Variant report

Variant rs72988166
Chromosome Location chr3:139942918-139942919
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:139938600-139944000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr3:139938600-139953600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr3:139941800-139943000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr3:139941800-139943200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr3:139941800-139943200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr3:139942000-139943000 Enhancers Muscle Satellite Cultured Cells --
7 chr3:139942000-139943400 Enhancers HMEC breast
8 chr3:139942200-139943000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr3:139942200-139943000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr3:139942200-139943000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:139942600-139944800 Weak transcription HSMM muscle
12 chr3:139942800-139952000 Weak transcription HSMMtube muscle

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