Variant report

Variant rs57688665
Chromosome Location chr21:29066227-29066228
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:29064000-29066400 Enhancers HUES48 Cell Line embryonic stem cell
2 chr21:29064800-29067400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr21:29065800-29067000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr21:29065800-29073600 Weak transcription HSMMtube muscle
5 chr21:29066000-29066400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr21:29066200-29066600 Weak transcription HMEC breast
7 chr21:29066200-29066800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr21:29066200-29066800 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr21:29066200-29067000 Weak transcription HSMM muscle
10 chr21:29066200-29067200 Enhancers Osteobl bone
11 chr21:29066200-29067400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr21:29066200-29072400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr21:29066200-29072400 Weak transcription Muscle Satellite Cultured Cells --
14 chr21:29066200-29072800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr21:29066200-29072800 Weak transcription NHDF-Ad bronchial
16 chr21:29066200-29073600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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