The 2.0 version of rSNPBase

Variant report

Variant rs2170858
Chromosome Location chr1:185757521-185757522
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:185737800-185758800 Weak transcription Fetal Lung lung
2 chr1:185753600-185757600 Weak transcription Right Atrium heart
3 chr1:185753600-185759600 Weak transcription Pancreas Pancrea
4 chr1:185755200-185758800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:185755200-185759400 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr1:185755200-185760000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr1:185755400-185766600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:185756000-185757600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:185756400-185761600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:185756600-185757800 Weak transcription Osteobl bone
11 chr1:185756600-185758400 Weak transcription Left Ventricle heart
12 chr1:185756800-185758200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr1:185756800-185758400 Weak transcription Aorta Aorta
14 chr1:185756800-185758400 Weak transcription Fetal Heart heart
15 chr1:185756800-185758800 Weak transcription NHDF-Ad bronchial
16 chr1:185757400-185758400 Weak transcription Breast Myoepithelial Primary Cells Breast

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Last update: Aug 31, 2015