Variant report

Variant rs17853460
Chromosome Location chr9:139943112-139943113
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139941200-139943200 Weak transcription K562 blood
2 chr9:139941200-139943400 Weak transcription HMEC breast
3 chr9:139941200-139943600 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:139941200-139944000 Weak transcription A549 lung
5 chr9:139941200-139944800 Bivalent Enhancer Placenta Placenta
6 chr9:139941200-139947800 Weak transcription Right Atrium heart
7 chr9:139941400-139943200 Weak transcription Gastric stomach
8 chr9:139941400-139943600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
9 chr9:139941600-139943200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
10 chr9:139942200-139944200 Weak transcription Hela-S3 cervix
11 chr9:139942400-139943200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr9:139942400-139943800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr9:139942600-139944800 Enhancers Pancreas Pancrea
14 chr9:139943000-139943800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
15 chr9:139943000-139944600 Bivalent Enhancer Fetal Muscle Leg muscle
16 chr9:139943000-139944800 Bivalent Enhancer Primary T cells fromperipheralblood blood

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