Variant report

Variant rs6809000
Chromosome Location chr3:17462036-17462037
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:17411200-17467400 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
2 chr3:17440800-17462400 Weak transcription Primary hematopoietic stem cells blood
3 chr3:17444200-17464800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr3:17448000-17476800 Weak transcription Primary B cells from peripheral blood blood
5 chr3:17448000-17506600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
6 chr3:17448400-17462200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr3:17459200-17462200 Weak transcription Fetal Kidney kidney
8 chr3:17460600-17475600 Weak transcription Fetal Intestine Small intestine
9 chr3:17461400-17462600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr3:17461600-17463000 Enhancers HepG2 liver
11 chr3:17461600-17463600 Enhancers Pancreatic Islets Pancreatic Islet
12 chr3:17461600-17476800 Weak transcription Primary B cells from cord blood blood
13 chr3:17461800-17462200 Weak transcription Pancreas Pancrea
14 chr3:17462000-17462400 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr3:17462000-17462800 Enhancers Liver Liver
16 chr3:17462000-17463400 Enhancers A549 lung

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