Variant report

Variant rs17163831
Chromosome Location chr1:223526993-223526994
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:223511800-223527000 Enhancers Fetal Heart heart
2 chr1:223514400-223535800 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr1:223517600-223527400 Enhancers Ovary ovary
4 chr1:223526200-223527000 Bivalent Enhancer Brain Angular Gyrus brain
5 chr1:223526200-223527200 Enhancers Brain Hippocampus Middle brain
6 chr1:223526400-223527400 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr1:223526600-223527600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr1:223526600-223530200 Weak transcription Esophagus oesophagus
9 chr1:223526600-223534000 Weak transcription Primary T cells from cord blood blood
10 chr1:223526800-223527000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr1:223526800-223527800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:223526800-223528000 Enhancers Liver Liver

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