The 2.0 version of rSNPBase

Variant report

Variant rs28496662
Chromosome Location chr8:49804613-49804614
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49800200-49806400 Weak transcription Fetal Lung lung
2 chr8:49802000-49809400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr8:49802000-49814800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr8:49803000-49806000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr8:49803200-49805600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:49803200-49805600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr8:49803600-49805400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr8:49803800-49804800 Enhancers HMEC breast
9 chr8:49803800-49805000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:49804200-49805800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr8:49804200-49811200 Weak transcription Fetal Kidney kidney
12 chr8:49804400-49805000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr8:49804400-49805000 Enhancers NHLF lung
14 chr8:49804400-49805400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr8:49804600-49806800 Weak transcription NHDF-Ad bronchial
16 chr8:49804600-49811400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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Last update: Aug 31, 2015