Variant report

Variant rs4887907
Chromosome Location chr16:77466321-77466322
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:77465200-77469200 Bivalent/Poised TSS Adipose Nuclei Adipose
2 chr16:77465400-77467200 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr16:77465600-77467200 Weak transcription Ovary ovary
4 chr16:77465800-77467200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr16:77466200-77466400 Flanking Active TSS Brain Cingulate Gyrus brain
6 chr16:77466200-77466400 Flanking Bivalent TSS/Enh HUVEC blood vessel
7 chr16:77466200-77466600 Bivalent Enhancer Fetal Kidney kidney
8 chr16:77466200-77467200 Enhancers Brain Substantia Nigra brain
9 chr16:77466200-77467400 Bivalent/Poised TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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