The 2.0 version of rSNPBase

Variant report

Variant rs3931243
Chromosome Location chr1:95235338-95235339
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:95221600-95239000 Weak transcription Fetal Intestine Large intestine
2 chr1:95223800-95241600 Weak transcription Aorta Aorta
3 chr1:95224000-95237800 Weak transcription NHLF lung
4 chr1:95224800-95237000 Weak transcription Pancreas Pancrea
5 chr1:95231400-95238000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:95233800-95238800 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr1:95234200-95236200 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr1:95234400-95237600 Weak transcription Primary neutrophils fromperipheralblood blood
9 chr1:95234600-95235600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:95234600-95236400 Enhancers Stomach Mucosa stomach
11 chr1:95234800-95235600 Enhancers Placenta Amnion Placenta Amnion
12 chr1:95234800-95235800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr1:95234800-95237200 Weak transcription Monocytes-CD14+_RO01746 blood
14 chr1:95234800-95239400 Weak transcription Fetal Intestine Small intestine
15 chr1:95235000-95235800 Enhancers NHEK skin
16 chr1:95235000-95237000 Weak transcription Primary monocytes fromperipheralblood blood
17 chr1:95235000-95237000 Weak transcription Lung lung

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Last update: Aug 31, 2015