Variant report

Variant rs11265947
Chromosome Location chr9:92492480-92492481
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:92465800-92507200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:92484000-92495000 Weak transcription Spleen Spleen
3 chr9:92488600-92496200 Weak transcription Fetal Heart heart
4 chr9:92489600-92497200 Enhancers Liver Liver
5 chr9:92491800-92506600 Enhancers Placenta Placenta
6 chr9:92492000-92493200 Enhancers Fetal Intestine Small intestine
7 chr9:92492000-92493400 Enhancers Esophagus oesophagus
8 chr9:92492000-92493600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr9:92492200-92492600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr9:92492200-92492600 Enhancers Duodenum Mucosa Duodenum
11 chr9:92492200-92492600 Enhancers Sigmoid Colon Sigmoid Colon
12 chr9:92492200-92492600 Enhancers NHEK skin
13 chr9:92492200-92493400 Enhancers Fetal Intestine Large intestine
14 chr9:92492400-92492600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr9:92492400-92493200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr9:92492400-92493200 Weak transcription Fetal Lung lung
17 chr9:92492400-92494600 Weak transcription Lung lung

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