Variant report

Variant rs73792076
Chromosome Location chr4:3452131-3452132
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3445800-3453600 Weak transcription Skeletal Muscle Female skeletal muscle
2 chr4:3449600-3452200 Weak transcription Spleen Spleen
3 chr4:3449800-3453800 Weak transcription Pancreas Pancrea
4 chr4:3450400-3452400 Weak transcription Brain Germinal Matrix brain
5 chr4:3450600-3452400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr4:3450800-3453000 Weak transcription Liver Liver
7 chr4:3451000-3452200 Bivalent Enhancer Fetal Stomach stomach
8 chr4:3451000-3452400 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr4:3451000-3453600 Weak transcription Fetal Brain Female brain
10 chr4:3451200-3452400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr4:3451200-3453800 Enhancers HepG2 liver
12 chr4:3451400-3452400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr4:3451400-3454200 Weak transcription Esophagus oesophagus
14 chr4:3451600-3452200 Enhancers Primary hematopoietic stem cells blood
15 chr4:3451600-3452200 Enhancers Primary hematopoietic stem cells short term culture blood
16 chr4:3451800-3452200 Bivalent Enhancer Fetal Muscle Leg muscle
17 chr4:3451800-3452200 Active TSS Gastric stomach
18 chr4:3452000-3452200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
19 chr4:3452000-3452400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
20 chr4:3452000-3453200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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