Variant report

Variant rs566971219
Chromosome Location chr7:17038483-17038484
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17031200-17047400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:17033400-17052600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr7:17033600-17043400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr7:17033800-17045200 Weak transcription Placenta Placenta
5 chr7:17038000-17038600 Enhancers Fetal Heart heart
6 chr7:17038400-17038600 Enhancers Esophagus oesophagus
7 chr7:17038400-17039400 Enhancers Primary neutrophils fromperipheralblood blood
8 chr7:17038400-17039400 Enhancers Monocytes-CD14+_RO01746 blood
9 chr7:17038400-17039800 Enhancers Primary monocytes fromperipheralblood blood
10 chr7:17038400-17040200 Enhancers Dnd41 blood

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