Variant report

Variant rs9306236
Chromosome Location chr22:20170093-20170094
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:20157600-20171400 Strong transcription Right Atrium heart
2 chr22:20167400-20172000 Enhancers Fetal Intestine Small intestine
3 chr22:20167400-20172400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr22:20168000-20171800 Enhancers Fetal Intestine Large intestine
5 chr22:20169200-20170200 Bivalent Enhancer Placenta Placenta
6 chr22:20169600-20174000 Weak transcription Liver Liver
7 chr22:20169800-20170400 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
8 chr22:20170000-20171000 Enhancers Spleen Spleen

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