The 2.0 version of rSNPBase

Variant report

Variant rs1856302
Chromosome Location chr1:169300818-169300819
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169260400-169310400 Weak transcription Fetal Stomach stomach
2 chr1:169265000-169320400 Weak transcription Aorta Aorta
3 chr1:169270200-169336400 Weak transcription Stomach Smooth Muscle stomach
4 chr1:169273600-169312400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr1:169276800-169304600 Weak transcription Ovary ovary
6 chr1:169277000-169306200 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr1:169280200-169304600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr1:169281600-169306600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr1:169282000-169306800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:169291000-169313200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:169294000-169305200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr1:169294600-169307400 Weak transcription Gastric stomach
13 chr1:169296400-169306600 Weak transcription Primary T killer memory cells from peripheral blood blood
14 chr1:169296600-169307600 Weak transcription A549 lung
15 chr1:169296600-169310400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:169296600-169324600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr1:169299800-169305000 Weak transcription Fetal Intestine Small intestine

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Last update: Aug 31, 2015