Variant report

Variant rs7859492
Chromosome Location chr9:102949286-102949287
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102935400-102952000 Weak transcription Small Intestine intestine
2 chr9:102936400-102952600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:102937800-102952000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:102938400-102950600 Weak transcription Liver Liver
5 chr9:102939600-102950800 Weak transcription Ovary ovary
6 chr9:102940200-102952000 Weak transcription Pancreas Pancrea
7 chr9:102940200-102959200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr9:102940400-102959200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr9:102940400-102978000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr9:102945800-102952000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:102948200-102957800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr9:102948400-102952000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:102949000-102952000 Weak transcription Primary B cells from cord blood blood

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