Variant report

Variant rs57741885
Chromosome Location chr12:31788664-31788665
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31783400-31789800 Weak transcription Placenta Placenta
2 chr12:31783400-31803000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr12:31783400-31803000 Weak transcription Fetal Intestine Small intestine
4 chr12:31783600-31792600 Weak transcription Pancreas Pancrea
5 chr12:31783800-31789600 Weak transcription Adipose Nuclei Adipose
6 chr12:31784600-31794000 Weak transcription Ovary ovary
7 chr12:31785400-31789000 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr12:31785600-31789000 Weak transcription Primary monocytes fromperipheralblood blood
9 chr12:31786000-31789000 Weak transcription Primary B cells from cord blood blood
10 chr12:31786000-31789400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr12:31788000-31793200 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr12:31788400-31789200 Enhancers Primary B cells from peripheral blood blood
13 chr12:31788400-31789200 Enhancers GM12878-XiMat blood

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