Variant report

Variant rs2279341
Chromosome Location chr19:41509950-41509951
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41507400-41529200 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr19:41508000-41511800 Strong transcription Liver Liver
3 chr19:41508000-41522400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr19:41509000-41510400 Enhancers Fetal Intestine Large intestine
5 chr19:41509200-41510400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr19:41509400-41510200 Flanking Active TSS Fetal Intestine Small intestine
7 chr19:41509600-41510200 Weak transcription Colonic Mucosa Colon
8 chr19:41509600-41510400 Enhancers H1 Cell Line embryonic stem cell
9 chr19:41509600-41510400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr19:41509800-41510400 Enhancers H9 Cell Line embryonic stem cell
11 chr19:41509800-41510400 Weak transcription iPS-15b Cell Line embryonic stem cell

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