Variant report

Variant rs2048973
Chromosome Location chr11:86839097-86839098
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86804600-86839400 Weak transcription Fetal Kidney kidney
2 chr11:86809000-86844000 Weak transcription Ovary ovary
3 chr11:86809000-86876000 Weak transcription Left Ventricle heart
4 chr11:86818200-86839200 Weak transcription Fetal Lung lung
5 chr11:86818200-86842800 Weak transcription Aorta Aorta
6 chr11:86818400-86842400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr11:86833400-86849400 Weak transcription Primary hematopoietic stem cells blood
8 chr11:86834600-86849800 Weak transcription Primary B cells from cord blood blood
9 chr11:86835200-86839200 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr11:86836200-86853000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr11:86836600-86839200 Weak transcription A549 lung
12 chr11:86836600-86848800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr11:86836800-86841200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr11:86836800-86877200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr11:86837200-86844000 Weak transcription Gastric stomach
16 chr11:86837200-86852600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr11:86838000-86840000 Enhancers HepG2 liver
18 chr11:86838600-86840800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
19 chr11:86838600-86846600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
20 chr11:86838800-86841600 Weak transcription Right Atrium heart
21 chr11:86839000-86839200 Enhancers Colon Smooth Muscle Colon
22 chr11:86839000-86839400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
23 chr11:86839000-86839400 Enhancers Stomach Mucosa stomach

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