Variant report

Variant rs7974863
Chromosome Location chr12:31784815-31784816
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31783400-31789800 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 chr12:31783600-31785000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr12:31783600-31785000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr12:31783600-31792600 Weak transcription Pancreas Pancrea
7 chr12:31783800-31785400 Weak transcription Fetal Adrenal Gland Adrenal Gland
8 chr12:31783800-31789600 Weak transcription Adipose Nuclei Adipose
9 chr12:31784000-31786200 Enhancers Primary B cells from peripheral blood blood
10 chr12:31784200-31786000 Enhancers Primary B cells from cord blood blood
11 chr12:31784400-31785600 Enhancers GM12878-XiMat blood
12 chr12:31784600-31785000 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr12:31784600-31785400 Enhancers Monocytes-CD14+_RO01746 blood
14 chr12:31784600-31794000 Weak transcription Ovary ovary
15 chr12:31784800-31785600 Enhancers Primary monocytes fromperipheralblood blood
16 chr12:31784800-31785600 Enhancers K562 blood
17 chr12:31784800-31788200 Weak transcription Fetal Heart heart

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