Variant report

Variant rs28496614
Chromosome Location chr8:49550534-49550535
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49534400-49556000 Weak transcription Pancreas Pancrea
2 chr8:49544400-49555400 Weak transcription Osteobl bone
3 chr8:49546600-49554400 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr8:49547200-49551200 Weak transcription Ovary ovary
5 chr8:49547400-49553400 Weak transcription Fetal Lung lung
6 chr8:49548400-49551200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr8:49548600-49551400 Enhancers HMEC breast
8 chr8:49548800-49550800 Enhancers NHEK skin
9 chr8:49549000-49550800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:49549400-49553400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr8:49550200-49555800 Enhancers Placenta Amnion Placenta Amnion
12 chr8:49550400-49552000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr8:49550400-49552800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr8:49550400-49552800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr8:49550400-49554200 Weak transcription Placenta Placenta
16 chr8:49550400-49556000 Weak transcription NH-A brain

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