Variant report

Variant rs7018703
Chromosome Location chr9:102952766-102952767
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102940200-102959200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr9:102940400-102959200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr9:102940400-102978000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr9:102948200-102957800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr9:102952000-102954000 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin
6 chr9:102952000-102954600 ZNF genes & repeats Primary B cells from cord blood blood
7 chr9:102952200-102953200 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
8 chr9:102952200-102953600 ZNF genes & repeats Adipose Nuclei Adipose
9 chr9:102952400-102952800 ZNF genes & repeats A549 lung
10 chr9:102952400-102954600 ZNF genes & repeats Fetal Lung lung
11 chr9:102952400-102963400 Weak transcription Pancreas Pancrea
12 chr9:102952600-102953000 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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