Variant report

Variant rs188664023
Chromosome Location chr9:139668640-139668641
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139667600-139669200 ZNF genes & repeats Fetal Intestine Small intestine
2 chr9:139668000-139669200 ZNF genes & repeats K562 blood
3 chr9:139668200-139668800 Enhancers Primary B cells from peripheral blood blood
4 chr9:139668200-139682400 Weak transcription Right Atrium heart
5 chr9:139668400-139668800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:139668600-139668800 Enhancers Fetal Thymus thymus
7 chr9:139668600-139668800 Enhancers HepG2 liver
8 chr9:139668600-139671400 Weak transcription Colonic Mucosa Colon

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