Variant report

Variant rs11118931
Chromosome Location chr1:222223013-222223014
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:222217400-222223800 Weak transcription Aorta Aorta
2 chr1:222218000-222227800 Weak transcription Brain Anterior Caudate brain
3 chr1:222220600-222223200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr1:222222400-222223400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:222222400-222229200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:222222600-222228200 Weak transcription Fetal Brain Male brain
7 chr1:222222800-222224000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
8 chr1:222222800-222224000 Weak transcription Colon Smooth Muscle Colon
9 chr1:222222800-222224200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:222222800-222224600 Weak transcription HMEC breast
11 chr1:222222800-222227400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr1:222222800-222227800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr1:222222800-222228600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:222222800-222232200 Weak transcription HSMM muscle
15 chr1:222223000-222225800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr1:222223000-222227800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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