Variant report

Variant rs829118
Chromosome Location chr12:51235317-51235318
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:51228400-51236600 Weak transcription Gastric stomach
2 chr12:51230800-51236000 Weak transcription Pancreas Pancrea
3 chr12:51233000-51236000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:51233400-51236600 Weak transcription Placenta Amnion Placenta Amnion
5 chr12:51233600-51236400 Enhancers Placenta Placenta
6 chr12:51234600-51235600 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr12:51234800-51235400 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
8 chr12:51235000-51236400 Weak transcription Esophagus oesophagus
9 chr12:51235000-51236800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr12:51235200-51236200 Weak transcription Pancreatic Islets Pancreatic Islet
11 chr12:51235200-51236200 Enhancers K562 blood
12 chr12:51235200-51236200 Weak transcription NHEK skin
13 chr12:51235200-51236400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr12:51235200-51236600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr12:51235200-51236600 Weak transcription Brain Cingulate Gyrus brain

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