Variant report

Variant rs17490208
Chromosome Location chr11:58422017-58422018
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58420600-58425600 Weak transcription HMEC breast
2 chr11:58421600-58422400 Enhancers Liver Liver
3 chr11:58421600-58422400 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr11:58421600-58422400 Enhancers Fetal Intestine Large intestine
5 chr11:58421600-58423000 Enhancers GM12878-XiMat blood
6 chr11:58421800-58422200 Enhancers Primary hematopoietic stem cells blood
7 chr11:58421800-58422200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr11:58421800-58422200 Enhancers HepG2 liver
9 chr11:58421800-58422200 Enhancers NHEK skin
10 chr11:58421800-58422400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:58421800-58422600 Enhancers Pancreas Pancrea
12 chr11:58422000-58426200 Weak transcription Fetal Intestine Small intestine

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