Variant report

Variant rs12553414
Chromosome Location chr9:139640033-139640034
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139636200-139640600 Active TSS Left Ventricle heart
2 chr9:139636600-139641200 Enhancers Spleen Spleen
3 chr9:139638000-139641200 Weak transcription Primary B cells from cord blood blood
4 chr9:139638000-139642600 Weak transcription Pancreas Pancrea
5 chr9:139638000-139642800 Weak transcription Fetal Heart heart
6 chr9:139638200-139641000 Weak transcription Esophagus oesophagus
7 chr9:139638200-139643400 Weak transcription Gastric stomach
8 chr9:139638600-139640400 Active TSS Right Ventricle heart
9 chr9:139639200-139640600 Active TSS Right Atrium heart
10 chr9:139639200-139642600 Weak transcription Primary hematopoietic stem cells short term culture blood
11 chr9:139639400-139643000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr9:139639600-139643200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr9:139639800-139640200 Enhancers Primary B cells from peripheral blood blood
14 chr9:139639800-139642600 Weak transcription Primary hematopoietic stem cells blood
15 chr9:139640000-139640200 Bivalent Enhancer Placenta Placenta
16 chr9:139640000-139640200 Flanking Active TSS Lung lung
17 chr9:139640000-139640200 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
18 chr9:139640000-139640400 Bivalent Enhancer HepG2 liver
19 chr9:139640000-139640600 Flanking Active TSS Adipose Nuclei Adipose
20 chr9:139640000-139640600 Bivalent/Poised TSS Stomach Smooth Muscle stomach
21 chr9:139640000-139640600 Flanking Active TSS K562 blood
22 chr9:139640000-139643400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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