Variant report

Variant rs530402425
Chromosome Location chr2:180061033-180061034
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180032200-180067600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:180055200-180066800 Weak transcription Fetal Kidney kidney
3 chr2:180056200-180066800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:180059600-180063400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:180060200-180066800 Weak transcription HepG2 liver
6 chr2:180060400-180061200 Enhancers Primary T cells fromperipheralblood blood
7 chr2:180060600-180061200 Active TSS H9 Cell Line embryonic stem cell
8 chr2:180060600-180061200 Enhancers Lung lung
9 chr2:180061000-180061200 Enhancers Primary Natural Killer cells fromperipheralblood blood

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