Variant report

Variant rs17726713
Chromosome Location chr2:210247729-210247730
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210246800-210248000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr2:210247200-210248600 Enhancers HMEC breast
3 chr2:210247200-210249000 Enhancers Placenta Amnion Placenta Amnion
4 chr2:210247400-210248600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:210247400-210248600 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr2:210247400-210248800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:210247400-210248800 Enhancers NHEK skin
8 chr2:210247600-210247800 Bivalent Enhancer Primary monocytes fromperipheralblood blood
9 chr2:210247600-210248400 Enhancers Hela-S3 cervix
10 chr2:210247600-210248600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:210247600-210248600 Enhancers HSMM muscle
12 chr2:210247600-210248800 Enhancers Pancreatic Islets Pancreatic Islet
13 chr2:210247600-210248800 Enhancers HUVEC blood vessel

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