Variant report

Variant rs56824662
Chromosome Location chr3:17466330-17466331
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr3:17448000-17476800 Weak transcription Primary B cells from peripheral blood blood
3 chr3:17448000-17506600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
4 chr3:17460600-17475600 Weak transcription Fetal Intestine Small intestine
5 chr3:17461600-17476800 Weak transcription Primary B cells from cord blood blood
6 chr3:17462400-17521400 Weak transcription Pancreas Pancrea
7 chr3:17465400-17466400 Enhancers GM12878-XiMat blood
8 chr3:17465400-17466800 Enhancers Fetal Heart heart
9 chr3:17465600-17466800 Enhancers A549 lung
10 chr3:17465600-17469800 Weak transcription Primary T killer naive cells fromperipheralblood blood
11 chr3:17465800-17466400 Enhancers Fetal Lung lung
12 chr3:17465800-17467600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr3:17465800-17468200 Weak transcription Spleen Spleen
14 chr3:17466000-17466400 Enhancers Pancreatic Islets Pancreatic Islet
15 chr3:17466000-17471000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr3:17466200-17466600 Weak transcription Small Intestine intestine
17 chr3:17466200-17472200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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