Variant report

Variant rs12342559
Chromosome Location chr9:139641732-139641733
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139638000-139642600 Weak transcription Pancreas Pancrea
2 chr9:139638000-139642800 Weak transcription Fetal Heart heart
3 chr9:139638200-139643400 Weak transcription Gastric stomach
4 chr9:139639200-139642600 Weak transcription Primary hematopoietic stem cells short term culture blood
5 chr9:139639400-139643000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr9:139639600-139643200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr9:139639800-139642600 Weak transcription Primary hematopoietic stem cells blood
8 chr9:139640000-139643400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr9:139640400-139642600 Weak transcription Lung lung
10 chr9:139640600-139642400 Weak transcription Left Ventricle heart
11 chr9:139640600-139643000 Weak transcription Right Atrium heart
12 chr9:139641000-139645800 Enhancers Primary B cells from peripheral blood blood
13 chr9:139641200-139642000 Weak transcription Spleen Spleen
14 chr9:139641200-139645400 Weak transcription K562 blood
15 chr9:139641400-139641800 Weak transcription Primary B cells from cord blood blood
16 chr9:139641400-139643800 Weak transcription Thymus Thymus
17 chr9:139641600-139641800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
18 chr9:139641600-139642000 Weak transcription Right Ventricle heart

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