Variant report

Variant rs6134741
Chromosome Location chr20:12970842-12970843
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:12966200-12978400 Weak transcription Fetal Intestine Large intestine
2 chr20:12969000-12971400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr20:12969200-12974400 Weak transcription Placenta Amnion Placenta Amnion
4 chr20:12969800-12977800 Weak transcription Placenta Placenta
5 chr20:12970400-12971600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr20:12970600-12971000 Enhancers HUES64 Cell Line embryonic stem cell
7 chr20:12970600-12971000 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr20:12970600-12971000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr20:12970600-12971000 Enhancers Fetal Brain Female brain
10 chr20:12970600-12971200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr20:12970800-12971200 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr20:12970800-12971800 Enhancers iPS-15b Cell Line embryonic stem cell

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