Variant report

Variant rs11808513
Chromosome Location chr1:186018677-186018678
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:185939200-186023000 Weak transcription Adipose Nuclei Adipose
2 chr1:185985400-186023800 Weak transcription Left Ventricle heart
3 chr1:185993200-186023000 Weak transcription Liver Liver
4 chr1:186001400-186019200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:186007400-186048000 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr1:186009400-186078000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:186012000-186048200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:186013000-186026600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:186013600-186068400 Weak transcription Fetal Kidney kidney
10 chr1:186015400-186019400 Weak transcription NH-A brain
11 chr1:186016200-186041800 Weak transcription Aorta Aorta
12 chr1:186016400-186023000 Weak transcription Fetal Lung lung
13 chr1:186016400-186038600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:186016800-186019400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:186017400-186019400 Weak transcription Hela-S3 cervix
16 chr1:186018600-186019000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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