Variant report

Variant rs2887269
Chromosome Location chr19:39252848-39252849
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39246400-39270800 Weak transcription K562 blood
2 chr19:39250200-39253800 Enhancers Fetal Intestine Large intestine
3 chr19:39250600-39253200 Weak transcription A549 lung
4 chr19:39251600-39259800 Weak transcription NHEK skin
5 chr19:39252200-39254000 Flanking Active TSS HepG2 liver
6 chr19:39252400-39253400 Weak transcription Fetal Intestine Small intestine
7 chr19:39252800-39253000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr19:39252800-39253200 Active TSS Liver Liver

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