Variant report

Variant rs10911865
Chromosome Location chr1:172498878-172498879
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172487800-172499000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr1:172492600-172499000 Weak transcription K562 blood
3 chr1:172495800-172500400 Weak transcription Fetal Intestine Small intestine
4 chr1:172498200-172500600 Enhancers HepG2 liver
5 chr1:172498200-172501200 Enhancers Placenta Amnion Placenta Amnion
6 chr1:172498400-172500600 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr1:172498800-172500400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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