Variant report

Variant rs1922946
Chromosome Location chr6:64972941-64972942
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:64970000-64974000 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr6:64971000-64973400 Enhancers HUES64 Cell Line embryonic stem cell
3 chr6:64972400-64973000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr6:64972400-64973000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:64972400-64973000 Enhancers Stomach Mucosa stomach
6 chr6:64972400-64973200 Active TSS GM12878-XiMat blood
7 chr6:64972400-64973800 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr6:64972400-64974400 Enhancers HUES48 Cell Line embryonic stem cell
9 chr6:64972600-64973400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr6:64972600-64973400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr6:64972600-64974400 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr6:64972600-64974400 Enhancers HUES6 Cell Line embryonic stem cell
13 chr6:64972800-64973000 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr6:64972800-64973000 Enhancers Fetal Intestine Small intestine

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