Variant report

Variant rs13373856
Chromosome Location chr1:220499565-220499566
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220493000-220499600 Weak transcription Fetal Heart heart
2 chr1:220498400-220500200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:220498800-220500000 Enhancers iPS-20b Cell Line embryonic stem cell
4 chr1:220498800-220500000 Enhancers HSMMtube muscle
5 chr1:220498800-220500200 Enhancers GM12878-XiMat blood
6 chr1:220498800-220503000 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr1:220499000-220500000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:220499000-220500200 Enhancers NH-A brain
9 chr1:220499000-220501600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr1:220499000-220502600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:220499000-220509400 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr1:220499200-220500000 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr1:220499200-220500600 Weak transcription Esophagus oesophagus

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