Variant report

Variant rs73649344
Chromosome Location chr9:92495150-92495151
allele C/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 chr9:92488600-92496200 Weak transcription Fetal Heart heart
3 chr9:92489600-92497200 Enhancers Liver Liver
4 chr9:92491800-92506600 Enhancers Placenta Placenta
5 chr9:92492600-92496200 Weak transcription Gastric stomach
6 chr9:92493400-92496400 Weak transcription Esophagus oesophagus
7 chr9:92493400-92496400 Weak transcription Placenta Amnion Placenta Amnion
8 chr9:92493600-92499000 Weak transcription Fetal Lung lung
9 chr9:92493600-92501400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:92494000-92495400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:92494600-92495200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr9:92494600-92495200 Enhancers Lung lung
13 chr9:92494600-92495400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr9:92495000-92495200 Enhancers Spleen Spleen
15 chr9:92495000-92495200 Bivalent Enhancer HepG2 liver
16 chr9:92495000-92496400 Weak transcription Fetal Intestine Small intestine
17 chr9:92495000-92499400 Weak transcription Fetal Intestine Large intestine

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