Variant report

Variant rs6475113
Chromosome Location chr9:17191399-17191400
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr9:17187600-17194800 Weak transcription Liver Liver
5 chr9:17189600-17193600 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr9:17189800-17192200 Weak transcription Primary monocytes fromperipheralblood blood
7 chr9:17190000-17193600 Weak transcription Fetal Muscle Leg muscle
8 chr9:17190600-17191400 Enhancers Fetal Lung lung
9 chr9:17191000-17191400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr9:17191000-17191400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:17191000-17191600 Enhancers HUVEC blood vessel
12 chr9:17191000-17192000 Enhancers Muscle Satellite Cultured Cells --
13 chr9:17191200-17191400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:17191200-17191600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr9:17191200-17191600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr9:17191200-17191600 Enhancers Colon Smooth Muscle Colon
17 chr9:17191200-17191600 Enhancers Fetal Heart heart
18 chr9:17191200-17191600 Enhancers Hela-S3 cervix
19 chr9:17191200-17191600 Enhancers Osteobl bone

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