Variant report

Variant rs2811863
Chromosome Location chr1:59200355-59200356
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59192600-59204200 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr1:59198000-59200600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:59198200-59201400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:59198200-59206200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:59198600-59205800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr1:59198800-59204000 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:59198800-59207200 Weak transcription Placenta Amnion Placenta Amnion
8 chr1:59200000-59200400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:59200200-59200400 Enhancers NHDF-Ad bronchial

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