Variant report

Variant rs138060127
Chromosome Location chr10:50815656-50815657
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:50815200-50815800 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
2 chr10:50815200-50815800 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr10:50815200-50815800 Bivalent Enhancer Placenta Placenta
4 chr10:50815200-50815800 Bivalent Enhancer Fetal Stomach stomach
5 chr10:50815200-50816800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
6 chr10:50815200-50816800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
7 chr10:50815200-50818000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
8 chr10:50815400-50815800 Bivalent Enhancer Brain Hippocampus Middle brain
9 chr10:50815400-50815800 Enhancers Spleen Spleen
10 chr10:50815600-50815800 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
11 chr10:50815600-50817000 Weak transcription Pancreas Pancrea
12 chr10:50815600-50817400 Bivalent Enhancer Cortex derived primary cultured neurospheres brain

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