Variant report

Variant rs10845038
Chromosome Location chr12:10248640-10248641
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10242800-10253800 Weak transcription Brain Hippocampus Middle brain
2 chr12:10245200-10248800 Weak transcription Left Ventricle heart
3 chr12:10245800-10251800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr12:10246200-10250000 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr12:10247200-10249400 Enhancers HUVEC blood vessel
6 chr12:10247800-10249000 Weak transcription Right Atrium heart
7 chr12:10247800-10250000 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr12:10247800-10250200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr12:10247800-10251600 Active TSS Adipose Nuclei Adipose
10 chr12:10247800-10252400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr12:10248200-10249600 Active TSS Duodenum Smooth Muscle Duodenum
12 chr12:10248400-10248800 Enhancers Psoas Muscle Psoas
13 chr12:10248600-10248800 Enhancers Placenta Amnion Placenta Amnion
14 chr12:10248600-10250200 Weak transcription Primary monocytes fromperipheralblood blood
15 chr12:10248600-10250200 Weak transcription Monocytes-CD14+_RO01746 blood

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