Variant report

Variant rs9813532
Chromosome Location chr3:17465704-17465705
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr3:17463600-17466000 Weak transcription Pancreatic Islets Pancreatic Islet
8 chr3:17464800-17465800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr3:17465000-17466200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr3:17465200-17466000 Enhancers Adipose Nuclei Adipose
11 chr3:17465400-17465800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr3:17465400-17466000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr3:17465400-17466400 Enhancers GM12878-XiMat blood
14 chr3:17465400-17466800 Enhancers Fetal Heart heart
15 chr3:17465600-17465800 Enhancers Spleen Spleen
16 chr3:17465600-17466000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr3:17465600-17466000 Enhancers Colon Smooth Muscle Colon
18 chr3:17465600-17466200 Enhancers Small Intestine intestine
19 chr3:17465600-17466200 Enhancers NHDF-Ad bronchial
20 chr3:17465600-17466800 Enhancers A549 lung
21 chr3:17465600-17469800 Weak transcription Primary T killer naive cells fromperipheralblood blood

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