Variant report

Variant rs6774882
Chromosome Location chr3:46491948-46491949
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:46455800-46496800 Strong transcription Primary neutrophils fromperipheralblood blood
2 chr3:46480200-46504000 Weak transcription Lung lung
3 chr3:46484800-46495000 Weak transcription Fetal Intestine Small intestine
4 chr3:46489200-46496800 Weak transcription Adipose Nuclei Adipose
5 chr3:46489400-46494800 Weak transcription Pancreas Pancrea
6 chr3:46489400-46504000 Weak transcription Right Atrium heart
7 chr3:46490200-46492600 Strong transcription Spleen Spleen
8 chr3:46490800-46494800 Weak transcription Gastric stomach
9 chr3:46491600-46492200 Enhancers Left Ventricle heart
10 chr3:46491600-46492200 Enhancers Skeletal Muscle Male skeletal muscle
11 chr3:46491600-46492600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr3:46491800-46492000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr3:46491800-46492400 Enhancers Right Ventricle heart
14 chr3:46491800-46492600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr3:46491800-46493000 Enhancers Placenta Amnion Placenta Amnion

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