Variant report

Variant rs6799026
Chromosome Location chr3:534800-534801
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:526800-543200 Weak transcription Aorta Aorta
2 chr3:533800-535000 Enhancers Fetal Intestine Large intestine
3 chr3:534000-535000 Enhancers H9 Cell Line embryonic stem cell
4 chr3:534000-535000 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr3:534200-534800 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr3:534200-534800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr3:534200-534800 Enhancers HUES48 Cell Line embryonic stem cell
8 chr3:534200-535000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr3:534200-535000 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr3:534200-535000 Flanking Active TSS Hela-S3 cervix
11 chr3:534400-534800 Flanking Active TSS Liver Liver
12 chr3:534400-534800 Enhancers Fetal Kidney kidney
13 chr3:534400-535000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr3:534600-534800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr3:534600-534800 Enhancers GM12878-XiMat blood
16 chr3:534800-535000 Enhancers Liver Liver
17 chr3:534800-540600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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