Variant report

Variant rs73554083
Chromosome Location chr9:139638457-139638458
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139636200-139640600 Active TSS Left Ventricle heart
2 chr9:139636400-139639800 Weak transcription K562 blood
3 chr9:139636600-139639200 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr9:139636600-139641200 Enhancers Spleen Spleen
5 chr9:139637000-139639200 Weak transcription Right Atrium heart
6 chr9:139637400-139638600 Enhancers Right Ventricle heart
7 chr9:139637400-139639600 Enhancers Primary B cells from peripheral blood blood
8 chr9:139637600-139639000 Weak transcription Primary hematopoietic stem cells blood
9 chr9:139637800-139639200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr9:139637800-139639200 Weak transcription Fetal Thymus thymus
11 chr9:139638000-139641200 Weak transcription Primary B cells from cord blood blood
12 chr9:139638000-139642600 Weak transcription Pancreas Pancrea
13 chr9:139638000-139642800 Weak transcription Fetal Heart heart
14 chr9:139638200-139639400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr9:139638200-139639600 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
16 chr9:139638200-139640000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr9:139638200-139641000 Weak transcription Esophagus oesophagus
18 chr9:139638200-139643400 Weak transcription Gastric stomach

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