Variant report

Variant rs566498113
Chromosome Location chr4:829092-829093
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:825600-831600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
2 chr4:826400-829200 Bivalent Enhancer Placenta Placenta
3 chr4:826400-829600 Enhancers Primary Natural Killer cells fromperipheralblood blood
4 chr4:826400-830600 Weak transcription Brain Germinal Matrix brain
5 chr4:826600-829600 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr4:827200-831600 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr4:827800-830200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
8 chr4:828400-830400 Enhancers Spleen Spleen
9 chr4:828800-829400 Strong transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr4:829000-829200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr4:829000-829200 Enhancers Esophagus oesophagus
12 chr4:829000-829400 Enhancers Stomach Mucosa stomach
13 chr4:829000-829600 Enhancers Gastric stomach
14 chr4:829000-829600 Bivalent Enhancer HepG2 liver
15 chr4:829000-830000 Enhancers Fetal Heart heart
16 chr4:829000-830000 Enhancers Left Ventricle heart
17 chr4:829000-830000 Enhancers Right Ventricle heart
18 chr4:829000-831000 Enhancers Pancreas Pancrea

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