Variant report

Variant rs1510962
Chromosome Location chr5:17406766-17406767
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17403000-17413000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr5:17404400-17407000 Enhancers Stomach Mucosa stomach
3 chr5:17404600-17411200 Weak transcription Fetal Brain Male brain
4 chr5:17404800-17406800 Enhancers HUES64 Cell Line embryonic stem cell
5 chr5:17405000-17406800 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr5:17405600-17407200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr5:17405800-17407200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr5:17406000-17407200 Enhancers HMEC breast
9 chr5:17406000-17407800 Enhancers Hela-S3 cervix
10 chr5:17406200-17406800 Active TSS Brain Inferior Temporal Lobe brain
11 chr5:17406200-17407000 Flanking Active TSS NHEK skin
12 chr5:17406400-17406800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr5:17406400-17407000 Flanking Active TSS A549 lung
14 chr5:17406400-17407200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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