Variant report

Variant rs9568570
Chromosome Location chr13:51906668-51906669
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51867600-51910800 Weak transcription Pancreas Pancrea
2 chr13:51900200-51914000 Weak transcription H9 Cell Line embryonic stem cell
3 chr13:51900400-51938200 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr13:51900800-51913400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr13:51903400-51913600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr13:51904000-51906800 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr13:51904000-51907800 Enhancers Fetal Thymus thymus
8 chr13:51904600-51907000 Enhancers Thymus Thymus
9 chr13:51904600-51907800 Enhancers Primary T cells from cord blood blood
10 chr13:51905000-51913800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr13:51905400-51915200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr13:51906000-51917200 Weak transcription HSMM muscle
13 chr13:51906000-51944400 Weak transcription Spleen Spleen
14 chr13:51906200-51907600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr13:51906200-51935400 Weak transcription HSMMtube muscle
16 chr13:51906600-51908600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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