Variant report

Variant rs9783500
Chromosome Location chr12:46899811-46899812
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46888600-46909200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:46893400-46911600 Weak transcription Osteobl bone
3 chr12:46899000-46900200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr12:46899200-46901400 ZNF genes & repeats NHEK skin
5 chr12:46899600-46900000 ZNF genes & repeats Primary B cells from cord blood blood
6 chr12:46899600-46900000 ZNF genes & repeats Primary B cells from peripheral blood blood
7 chr12:46899600-46900000 ZNF genes & repeats NH-A brain
8 chr12:46899600-46900400 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr12:46899600-46901200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr12:46899600-46901200 ZNF genes & repeats Primary hematopoietic stem cells blood
11 chr12:46899600-46901600 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
12 chr12:46899800-46901000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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