Variant report

Variant rs4752858
Chromosome Location chr11:47685829-47685830
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:47676800-47703400 Weak transcription Fetal Intestine Small intestine
2 chr11:47682000-47688600 Weak transcription HepG2 liver
3 chr11:47683200-47688200 Weak transcription Fetal Lung lung
4 chr11:47684400-47686800 Enhancers NHEK skin
5 chr11:47685000-47686200 Weak transcription Hela-S3 cervix
6 chr11:47685400-47686400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:47685600-47687200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr11:47685600-47688400 Weak transcription Fetal Stomach stomach
9 chr11:47685800-47687000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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