Variant report

Variant rs55773493
Chromosome Location chr6:44818045-44818046
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44798400-44822800 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr6:44808600-44821000 Weak transcription Primary T cells from cord blood blood
3 chr6:44817200-44820000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr6:44817400-44818400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr6:44817400-44819600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:44817600-44818400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr6:44817600-44818400 Enhancers HSMMtube muscle
8 chr6:44817600-44819400 Enhancers Muscle Satellite Cultured Cells --
9 chr6:44817600-44819600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr6:44817800-44818200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:44818000-44818600 Weak transcription HSMM muscle
12 chr6:44818000-44818800 Enhancers Fetal Stomach stomach
13 chr6:44818000-44832200 Weak transcription Primary Natural Killer cells fromperipheralblood blood

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