Variant report

Variant rs569339
Chromosome Location chr3:101029149-101029150
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:101026600-101029400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr3:101028000-101044200 Weak transcription Primary T cells fromperipheralblood blood
3 chr3:101028400-101030800 Enhancers Fetal Kidney kidney
4 chr3:101028800-101029600 Weak transcription HUVEC blood vessel
5 chr3:101028800-101030200 Enhancers Muscle Satellite Cultured Cells --
6 chr3:101028800-101031000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr3:101028800-101032800 Weak transcription Primary T helper naive cells from peripheral blood blood
8 chr3:101029000-101029200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr3:101029000-101029200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr3:101029000-101029400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr3:101029000-101029400 Enhancers Ovary ovary
12 chr3:101029000-101029400 Enhancers Osteobl bone
13 chr3:101029000-101029800 Strong transcription Primary T cells from cord blood blood
14 chr3:101029000-101030200 Enhancers Fetal Stomach stomach
15 chr3:101029000-101030800 Enhancers Colon Smooth Muscle Colon
16 chr3:101029000-101030800 Enhancers Rectal Smooth Muscle rectum

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