Variant report

Variant rs6650636
Chromosome Location chr18:28796618-28796619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28787200-28805600 Weak transcription Pancreas Pancrea
2 chr18:28787600-28797000 Weak transcription Right Atrium heart
3 chr18:28791400-28796800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr18:28791400-28796800 Weak transcription Left Ventricle heart
5 chr18:28791400-28805600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr18:28792400-28796800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr18:28796400-28798000 Enhancers HepG2 liver
8 chr18:28796600-28796800 Enhancers Fetal Kidney kidney
9 chr18:28796600-28797000 Enhancers Stomach Mucosa stomach
10 chr18:28796600-28798000 Enhancers HUES6 Cell Line embryonic stem cell
11 chr18:28796600-28798000 Enhancers Placenta Placenta

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