The 2.0 version of rSNPBase

Variant report

Variant rs73049479
Chromosome Location chr1:180623481-180623482
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180602000-180645200 Weak transcription Gastric stomach
2 chr1:180603600-180626400 Weak transcription Fetal Lung lung
3 chr1:180605600-180625800 Weak transcription Primary T killer memory cells from peripheral blood blood
4 chr1:180605800-180625000 Weak transcription Primary T helper cells fromperipheralblood blood
5 chr1:180609800-180625800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:180612800-180626400 Weak transcription Primary hematopoietic stem cells blood
7 chr1:180613200-180632600 Weak transcription Aorta Aorta
8 chr1:180613400-180626400 Weak transcription Adipose Nuclei Adipose
9 chr1:180613400-180626600 Weak transcription Duodenum Smooth Muscle Duodenum
10 chr1:180615600-180623800 Weak transcription Primary B cells from cord blood blood
11 chr1:180616200-180624800 Weak transcription Primary T cells from cord blood blood
12 chr1:180616400-180627200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:180616600-180624400 Weak transcription K562 blood
14 chr1:180616600-180626000 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr1:180619600-180632600 Weak transcription Pancreas Pancrea
16 chr1:180619600-180634600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
17 chr1:180622400-180626400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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Last update: Aug 31, 2015