Variant report

Variant rs7762789
Chromosome Location chr6:167149090-167149091
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167136600-167157600 Weak transcription Brain Angular Gyrus brain
2 chr6:167142600-167149200 Weak transcription H1 Cell Line embryonic stem cell
3 chr6:167142800-167153000 Weak transcription Lung lung
4 chr6:167142800-167156600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:167143000-167150400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:167143200-167152800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
7 chr6:167146400-167151800 Weak transcription Stomach Smooth Muscle stomach
8 chr6:167147600-167153200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr6:167147800-167149800 Weak transcription NHEK skin
10 chr6:167147800-167150600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:167147800-167153000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr6:167148000-167149600 Enhancers Primary neutrophils fromperipheralblood blood
13 chr6:167148000-167149600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr6:167148000-167149800 Weak transcription HUES64 Cell Line embryonic stem cell
15 chr6:167148200-167149600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr6:167148200-167149800 Weak transcription ES-WA7 Cell Line embryonic stem cell

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