Variant report

Variant rs829116
Chromosome Location chr12:51232914-51232915
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:51228400-51235200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr12:51228400-51236600 Weak transcription Gastric stomach
3 chr12:51230800-51236000 Weak transcription Pancreas Pancrea
4 chr12:51232400-51233000 Enhancers NHDF-Ad bronchial
5 chr12:51232400-51233400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr12:51232400-51233400 Enhancers Fetal Brain Male brain
7 chr12:51232400-51233400 Enhancers Placenta Amnion Placenta Amnion
8 chr12:51232600-51233400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr12:51232600-51233400 Enhancers NHEK skin
10 chr12:51232800-51233000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr12:51232800-51233200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr12:51232800-51233200 Enhancers Osteobl bone
13 chr12:51232800-51234800 Weak transcription Pancreatic Islets Pancreatic Islet

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