Variant report

Variant rs6688298
Chromosome Location chr1:185756573-185756574
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr1:185755200-185756800 Enhancers NHDF-Ad bronchial
5 chr1:185755200-185758800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:185755200-185759400 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr1:185755200-185760000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:185755400-185756600 Enhancers Osteobl bone
9 chr1:185755400-185766600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:185755600-185756800 Enhancers Aorta Aorta
11 chr1:185756000-185757600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr1:185756200-185756600 Enhancers Fetal Brain Male brain
13 chr1:185756200-185756800 Enhancers Fetal Heart heart
14 chr1:185756400-185756600 Bivalent Enhancer Gastric stomach
15 chr1:185756400-185756600 Enhancers Left Ventricle heart
16 chr1:185756400-185756800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
17 chr1:185756400-185761600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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