Variant report

Variant rs2800849
Chromosome Location chr1:222224354-222224355
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:222218000-222227800 Weak transcription Brain Anterior Caudate brain
2 chr1:222222400-222229200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr1:222222600-222228200 Weak transcription Fetal Brain Male brain
4 chr1:222222800-222224600 Weak transcription HMEC breast
5 chr1:222222800-222227400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:222222800-222227800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:222222800-222228600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:222222800-222232200 Weak transcription HSMM muscle
9 chr1:222223000-222225800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr1:222223000-222227800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr1:222223400-222224800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr1:222224000-222224800 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr1:222224200-222224400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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