Variant report

Variant rs141134821
Chromosome Location chr6:32355795-32355796
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:32344000-32361400 Weak transcription Fetal Stomach stomach
2 chr6:32351400-32365000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr6:32354800-32356000 Enhancers GM12878-XiMat blood
4 chr6:32354800-32356200 Enhancers Fetal Intestine Small intestine
5 chr6:32355000-32356000 Enhancers Primary B cells from peripheral blood blood
6 chr6:32355000-32356400 Enhancers Duodenum Mucosa Duodenum
7 chr6:32355200-32356200 Enhancers Stomach Mucosa stomach
8 chr6:32355400-32356000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr6:32355400-32356200 Enhancers Fetal Intestine Large intestine
10 chr6:32355600-32358000 Weak transcription Primary hematopoietic stem cells short term culture blood

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