Variant report

Variant rs35855940
Chromosome Location chr19:39235103-39235104
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39233000-39235200 Enhancers HepG2 liver
2 chr19:39233200-39236000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr19:39234200-39235400 Enhancers Spleen Spleen
4 chr19:39234400-39235200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr19:39234400-39235200 Enhancers A549 lung
6 chr19:39234400-39236000 Enhancers K562 blood
7 chr19:39234600-39235200 Enhancers Placenta Placenta
8 chr19:39234800-39235200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
9 chr19:39235000-39235200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
10 chr19:39235000-39235600 Enhancers Primary T cells fromperipheralblood blood

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