Variant report

Variant rs10117822
Chromosome Location chr9:139602652-139602653
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139593800-139605600 Weak transcription Liver Liver
2 chr9:139596200-139606200 Weak transcription Fetal Intestine Small intestine
3 chr9:139596400-139606200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:139596400-139606200 Weak transcription Spleen Spleen
5 chr9:139598200-139604000 Weak transcription Thymus Thymus
6 chr9:139600200-139606000 Weak transcription Adipose Nuclei Adipose
7 chr9:139600800-139604600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr9:139600800-139605000 Weak transcription Primary hematopoietic stem cells blood
9 chr9:139600800-139605000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr9:139602000-139603800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:139602400-139603000 Flanking Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
12 chr9:139602600-139602800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr9:139602600-139603000 Flanking Bivalent TSS/Enh HepG2 liver
14 chr9:139602600-139603000 Enhancers K562 blood

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