Variant report

Variant rs2477231
Chromosome Location chr6:33892563-33892564
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33886600-33894600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:33889800-33893200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:33890600-33892600 Enhancers Primary hematopoietic stem cells blood
4 chr6:33890600-33893400 Enhancers Fetal Thymus thymus
5 chr6:33891600-33893400 Enhancers Pancreas Pancrea
6 chr6:33891600-33893800 Enhancers Spleen Spleen
7 chr6:33891800-33893000 Weak transcription Fetal Lung lung
8 chr6:33891800-33894000 Enhancers Ovary ovary
9 chr6:33892000-33892800 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
10 chr6:33892200-33892600 Enhancers Fetal Brain Female brain
11 chr6:33892200-33895600 Enhancers Brain Germinal Matrix brain
12 chr6:33892400-33893000 Bivalent Enhancer Fetal Stomach stomach
13 chr6:33892400-33894200 Enhancers Fetal Brain Male brain

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