Variant report

Variant rs11039329
Chromosome Location chr11:47684908-47684909
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 chr11:47684600-47685000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr11:47684600-47685000 Enhancers GM12878-XiMat blood
7 chr11:47684600-47685000 Enhancers Hela-S3 cervix
8 chr11:47684800-47685000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:47684800-47685000 Enhancers HUVEC blood vessel

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