Variant report

Variant rs28507639
Chromosome Location chr4:121778956-121778957
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:121756800-121779800 Weak transcription Aorta Aorta
2 chr4:121761200-121783600 Weak transcription Pancreas Pancrea
3 chr4:121765800-121786600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr4:121766000-121786600 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr4:121766200-121790800 Weak transcription Ovary ovary
6 chr4:121769000-121779600 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr4:121769200-121779600 Weak transcription Fetal Muscle Trunk muscle
8 chr4:121771400-121781200 Weak transcription HSMM muscle
9 chr4:121771600-121783200 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr4:121771800-121779600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr4:121771800-121786800 Weak transcription Fetal Lung lung
12 chr4:121774400-121780400 Enhancers NHDF-Ad bronchial
13 chr4:121775200-121779200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:121775200-121790800 Weak transcription Fetal Kidney kidney
15 chr4:121775400-121780000 Weak transcription Muscle Satellite Cultured Cells --
16 chr4:121776800-121779400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
17 chr4:121777000-121783600 Weak transcription Fetal Intestine Small intestine
18 chr4:121778600-121779200 Enhancers NHLF lung
19 chr4:121778600-121780200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
20 chr4:121778800-121779000 Enhancers HUES48 Cell Line embryonic stem cell
21 chr4:121778800-121779200 Weak transcription Fetal Heart heart

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