Variant report

Variant rs4846315
Chromosome Location chr1:220498903-220498904
allele C/T
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 chr1:220498400-220499000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:220498400-220499000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr1:220498400-220500200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:220498800-220499000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:220498800-220499000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:220498800-220499000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr1:220498800-220499000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:220498800-220499200 Enhancers Esophagus oesophagus
10 chr1:220498800-220500000 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr1:220498800-220500000 Enhancers HSMMtube muscle
12 chr1:220498800-220500200 Enhancers GM12878-XiMat blood
13 chr1:220498800-220503000 Weak transcription Cortex derived primary cultured neurospheres brain

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