Variant report

Variant rs16981008
Chromosome Location chr21:29066614-29066615
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:29064800-29067400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr21:29065800-29067000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr21:29065800-29073600 Weak transcription HSMMtube muscle
4 chr21:29066200-29066800 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr21:29066200-29066800 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr21:29066200-29067000 Weak transcription HSMM muscle
7 chr21:29066200-29067200 Enhancers Osteobl bone
8 chr21:29066200-29067400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr21:29066200-29072400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr21:29066200-29072400 Weak transcription Muscle Satellite Cultured Cells --
11 chr21:29066200-29072800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr21:29066200-29072800 Weak transcription NHDF-Ad bronchial
13 chr21:29066200-29073600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr21:29066400-29066800 Weak transcription HUES48 Cell Line embryonic stem cell
15 chr21:29066400-29067200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr21:29066600-29067600 Enhancers HMEC breast

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