Variant report

Variant rs142718588
Chromosome Location chr11:33384302-33384303
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33372000-33392400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:33375200-33392600 Weak transcription Pancreas Pancrea
3 chr11:33375800-33388400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr11:33376200-33386400 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
5 chr11:33376800-33390800 Weak transcription NH-A brain
6 chr11:33380600-33397000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:33383000-33384400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr11:33383600-33384400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr11:33383600-33384400 Enhancers Primary T helper cells PMA-I stimulated --
10 chr11:33383600-33384400 Enhancers Primary Natural Killer cells fromperipheralblood blood
11 chr11:33383600-33384400 Enhancers Muscle Satellite Cultured Cells --
12 chr11:33383800-33384600 Weak transcription HMEC breast
13 chr11:33384000-33388400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr11:33384000-33393000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr11:33384000-33393000 Weak transcription A549 lung
16 chr11:33384000-33394200 Weak transcription HSMMtube muscle

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