Variant report

Variant rs11145907
Chromosome Location chr9:139763503-139763504
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139761400-139763800 Weak transcription Brain Inferior Temporal Lobe brain
2 chr9:139761400-139764800 Weak transcription Brain Hippocampus Middle brain
3 chr9:139761600-139764200 Weak transcription Fetal Lung lung
4 chr9:139761800-139766400 Weak transcription Thymus Thymus
5 chr9:139761800-139766600 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr9:139762000-139763600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
7 chr9:139762000-139763800 Weak transcription Skeletal Muscle Male skeletal muscle
8 chr9:139762000-139764400 Weak transcription Brain Cingulate Gyrus brain
9 chr9:139762000-139765800 Weak transcription Muscle Satellite Cultured Cells --
10 chr9:139762200-139765600 Weak transcription Primary hematopoietic stem cells blood
11 chr9:139762200-139769400 Weak transcription K562 blood
12 chr9:139762400-139763600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin
13 chr9:139762600-139765000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr9:139762600-139766400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:139763200-139763600 Enhancers Pancreas Pancrea
16 chr9:139763400-139763600 Weak transcription Gastric stomach
17 chr9:139763400-139763800 Enhancers Hela-S3 cervix
18 chr9:139763400-139764800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr9:139763400-139767000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
20 chr9:139763400-139771200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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