Variant report

Variant rs55977965
Chromosome Location chr2:181882885-181882886
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181856800-181897200 Weak transcription Primary B cells from cord blood blood
2 chr2:181857800-181901200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:181860000-181894800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:181871000-181886600 Weak transcription Brain Hippocampus Middle brain
5 chr2:181873200-181885000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:181873400-181901000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:181873600-181887800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:181873600-181889600 Weak transcription Colon Smooth Muscle Colon
9 chr2:181876200-181885000 Weak transcription Brain Angular Gyrus brain
10 chr2:181878800-181883800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:181882200-181883600 Weak transcription Left Ventricle heart
12 chr2:181882200-181885000 Weak transcription Psoas Muscle Psoas
13 chr2:181882400-181884800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr2:181882600-181883400 Enhancers Duodenum Smooth Muscle Duodenum
15 chr2:181882800-181883400 Enhancers Pancreatic Islets Pancreatic Islet

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