The 2.0 version of rSNPBase

Variant report

Variant rs73974706
Chromosome Location chr2:181882338-181882339
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr2:181877600-181882800 Weak transcription Pancreatic Islets Pancreatic Islet
11 chr2:181878800-181883800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:181881800-181882400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr2:181882200-181882600 Weak transcription Duodenum Smooth Muscle Duodenum
14 chr2:181882200-181882800 Enhancers Primary T helper naive cells from peripheral blood blood
15 chr2:181882200-181883600 Weak transcription Left Ventricle heart
16 chr2:181882200-181885000 Weak transcription Psoas Muscle Psoas

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Last update: Aug 31, 2015