Variant report

Variant rs1894692
Chromosome Location chr1:169467654-169467655
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169465200-169468000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:169465600-169468600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:169465800-169468800 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr1:169467000-169467800 Enhancers Placenta Amnion Placenta Amnion
5 chr1:169467000-169469000 Enhancers Placenta Placenta
6 chr1:169467400-169467800 Weak transcription HepG2 liver
7 chr1:169467400-169468000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr1:169467600-169467800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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