Variant report

Variant rs10845039
Chromosome Location chr12:10249098-10249099
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10242800-10253800 Weak transcription Brain Hippocampus Middle brain
2 chr12:10245800-10251800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr12:10246200-10250000 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr12:10247200-10249400 Enhancers HUVEC blood vessel
5 chr12:10247800-10250000 Weak transcription Primary neutrophils fromperipheralblood blood
6 chr12:10247800-10250200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr12:10247800-10251600 Active TSS Adipose Nuclei Adipose
8 chr12:10247800-10252400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr12:10248200-10249600 Active TSS Duodenum Smooth Muscle Duodenum
10 chr12:10248600-10250200 Weak transcription Primary monocytes fromperipheralblood blood
11 chr12:10248600-10250200 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr12:10248800-10249400 Active TSS Lung lung
13 chr12:10248800-10251200 Weak transcription Placenta Amnion Placenta Amnion
14 chr12:10248800-10251600 Active TSS Left Ventricle heart
15 chr12:10248800-10251600 Active TSS Psoas Muscle Psoas
16 chr12:10249000-10251600 Active TSS Right Ventricle heart
17 chr12:10249000-10252000 Active TSS Right Atrium heart

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