The 2.0 version of rSNPBase

Variant report

Variant rs506429
Chromosome Location chr1:185542381-185542382
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:185529400-185543000 Weak transcription Pancreas Pancrea
2 chr1:185530800-185544000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:185534800-185543000 Weak transcription A549 lung
4 chr1:185535000-185543400 Weak transcription HSMMtube muscle
5 chr1:185537200-185543000 Weak transcription Small Intestine intestine
6 chr1:185538600-185542800 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr1:185538800-185542400 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr1:185539000-185542400 Weak transcription Primary monocytes fromperipheralblood blood
9 chr1:185540200-185543000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:185540400-185542800 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr1:185540400-185543000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:185540600-185543000 Weak transcription HMEC breast
13 chr1:185540600-185551200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:185540800-185543000 Weak transcription NHEK skin
15 chr1:185541600-185542600 Weak transcription Fetal Intestine Small intestine
16 chr1:185542000-185543000 Weak transcription Placenta Amnion Placenta Amnion
17 chr1:185542000-185543800 Enhancers Fetal Kidney kidney
18 chr1:185542000-185544000 Enhancers Primary neutrophils fromperipheralblood blood
19 chr1:185542000-185544200 Enhancers Primary B cells from peripheral blood blood
20 chr1:185542200-185544400 Enhancers Fetal Intestine Large intestine

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Last update: Aug 31, 2015