Variant report

Variant rs73547538
Chromosome Location chr9:99834803-99834804
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:99833400-99835000 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr9:99833400-99835200 Enhancers Fetal Intestine Large intestine
3 chr9:99833800-99835000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:99834200-99835200 Enhancers Fetal Intestine Small intestine
5 chr9:99834400-99835000 Bivalent Enhancer HepG2 liver
6 chr9:99834400-99835200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr9:99834400-99835200 Enhancers Placenta Placenta
8 chr9:99834400-99835200 Enhancers NHEK skin
9 chr9:99834400-99835400 Enhancers Fetal Heart heart
10 chr9:99834400-99835400 Bivalent Enhancer Hela-S3 cervix
11 chr9:99834400-99835600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr9:99834600-99835200 Enhancers H1 Cell Line embryonic stem cell
13 chr9:99834600-99835200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:99834600-99835400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr9:99834600-99835400 Enhancers H9 Cell Line embryonic stem cell

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