Variant report

Variant rs1013070
Chromosome Location chr21:39995459-39995460
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:39989200-39997600 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr21:39993200-39995600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr21:39993200-39996600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr21:39993800-39995600 Enhancers HepG2 liver
5 chr21:39994600-39995600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr21:39994600-39995600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr21:39994600-39996000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr21:39994600-39996000 Weak transcription Aorta Aorta
9 chr21:39994800-39996000 Weak transcription Spleen Spleen
10 chr21:39995200-39996000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr21:39995200-39999200 Weak transcription Gastric stomach
12 chr21:39995200-40002400 Weak transcription H9 Cell Line embryonic stem cell
13 chr21:39995400-39995800 Enhancers Fetal Kidney kidney
14 chr21:39995400-39996600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr21:39995400-39996600 Enhancers Ovary ovary

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