Variant report

Variant rs10962896
Chromosome Location chr9:17190094-17190095
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17159800-17195600 Weak transcription Aorta Aorta
2 chr9:17172200-17193600 Weak transcription Pancreas Pancrea
3 chr9:17179000-17204400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr9:17185800-17191200 Weak transcription Fetal Heart heart
5 chr9:17186000-17190600 Weak transcription Fetal Lung lung
6 chr9:17187600-17194800 Weak transcription Liver Liver
7 chr9:17188600-17190600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr9:17189600-17193600 Weak transcription Primary hematopoietic stem cells short term culture blood
9 chr9:17189800-17190200 Enhancers Spleen Spleen
10 chr9:17189800-17192200 Weak transcription Primary monocytes fromperipheralblood blood
11 chr9:17190000-17190600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr9:17190000-17193600 Weak transcription Fetal Muscle Leg muscle

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