Variant report

Variant rs4931527
Chromosome Location chr12:31783660-31783661
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31782200-31784600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr12:31782400-31783800 Enhancers Adipose Nuclei Adipose
3 chr12:31782400-31783800 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr12:31782400-31784000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr12:31782400-31784000 Enhancers Fetal Stomach stomach
6 chr12:31782400-31784000 Enhancers Left Ventricle heart
7 chr12:31782400-31784000 Enhancers HSMM muscle
8 chr12:31782400-31784600 Enhancers Fetal Muscle Leg muscle
9 chr12:31783200-31784000 Enhancers Fetal Kidney kidney
10 chr12:31783400-31783800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr12:31783400-31784600 Enhancers Ovary ovary
12 chr12:31783400-31784800 Enhancers Fetal Heart heart
13 chr12:31783400-31789800 Weak transcription Placenta Placenta
14 chr12:31783400-31803000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr12:31783400-31803000 Weak transcription Fetal Intestine Small intestine
16 chr12:31783600-31784200 Enhancers Stomach Smooth Muscle stomach
17 chr12:31783600-31784800 Weak transcription K562 blood
18 chr12:31783600-31785000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr12:31783600-31785000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
20 chr12:31783600-31792600 Weak transcription Pancreas Pancrea

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