Variant report

Variant rs1198329
Chromosome Location chr13:50390096-50390097
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50384200-50390200 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr13:50386000-50390400 Enhancers HepG2 liver
3 chr13:50387400-50394600 Weak transcription H9 Cell Line embryonic stem cell
4 chr13:50387400-50394800 Weak transcription Fetal Intestine Large intestine
5 chr13:50388800-50390200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
6 chr13:50389400-50390200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr13:50389400-50392800 Weak transcription Fetal Heart heart
8 chr13:50390000-50394800 Weak transcription Placenta Placenta

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