Variant report

Variant rs16962736
Chromosome Location chr15:49965867-49965868
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:49961800-49966800 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr15:49962000-49966600 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr15:49962400-49966600 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr15:49962400-49966800 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr15:49962800-49966800 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr15:49963200-49967000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr15:49965400-49968400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr15:49965600-49966600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr15:49965600-49967000 Enhancers A549 lung
10 chr15:49965600-49967200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr15:49965600-49968000 Enhancers Hela-S3 cervix
12 chr15:49965600-49968200 Enhancers HMEC breast
13 chr15:49965600-49968600 Enhancers NHDF-Ad bronchial
14 chr15:49965800-49967600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr15:49965800-49967800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr15:49965800-49967800 Enhancers NHEK skin
17 chr15:49965800-49968200 Enhancers Osteobl bone

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