Variant report

Variant rs58006748
Chromosome Location chr11:18921484-18921485
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:18915200-18922000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr11:18920800-18923000 Enhancers HepG2 liver
3 chr11:18921000-18921800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr11:18921000-18922200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr11:18921000-18922200 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr11:18921200-18922400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:18921200-18922400 Enhancers HMEC breast
8 chr11:18921200-18922600 Enhancers NHEK skin
9 chr11:18921400-18921600 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr11:18921400-18921800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:18921400-18922400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr11:18921400-18922600 Enhancers iPS-18 Cell Line embryonic stem cell

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