Variant report

Variant rs7894644
Chromosome Location chr10:4929940-4929941
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:4908800-4944200 Weak transcription Adipose Nuclei Adipose
2 chr10:4910400-4936400 Weak transcription Left Ventricle heart
3 chr10:4915800-4943600 Weak transcription Aorta Aorta
4 chr10:4916800-4936400 Weak transcription Pancreas Pancrea
5 chr10:4918400-4968000 Weak transcription Primary T cells from cord blood blood
6 chr10:4918800-4931400 Weak transcription Duodenum Mucosa Duodenum
7 chr10:4919200-4936800 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr10:4921600-4930800 Weak transcription Stomach Smooth Muscle stomach
9 chr10:4925600-4930200 Strong transcription Liver Liver
10 chr10:4925800-4936400 Weak transcription Right Atrium heart
11 chr10:4926200-4931400 Weak transcription HepG2 liver
12 chr10:4927400-4930200 Enhancers Primary hematopoietic stem cells blood
13 chr10:4927800-4936200 Weak transcription Lung lung
14 chr10:4929200-4930000 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr10:4929200-4930000 Active TSS Primary T regulatory cells fromperipheralblood blood
16 chr10:4929200-4930200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr10:4929200-4932200 Enhancers Fetal Stomach stomach
18 chr10:4929400-4930000 Enhancers Fetal Muscle Leg muscle
19 chr10:4929600-4930000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
20 chr10:4929800-4930000 Flanking Active TSS Primary B cells from cord blood blood
21 chr10:4929800-4931200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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