The 2.0 version of rSNPBase

Variant report

Variant rs35313719
Chromosome Location chr11:26214782-26214783
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26211000-26216200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr11:26211200-26216600 Weak transcription Fetal Kidney kidney
3 chr11:26211600-26214800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr11:26211600-26216800 Weak transcription Osteobl bone
5 chr11:26211600-26220600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr11:26211800-26220200 Weak transcription NHLF lung
7 chr11:26212400-26217200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr11:26212400-26225000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:26212600-26217000 Weak transcription Adipose Nuclei Adipose
10 chr11:26212600-26219400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr11:26212600-26220600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr11:26213200-26215200 Weak transcription NHDF-Ad bronchial
13 chr11:26214200-26215200 Enhancers Placenta Placenta
14 chr11:26214600-26215000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr11:26214600-26216600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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Last update: Aug 31, 2015