Variant report

Variant rs188610
Chromosome Location chr12:313839-313840
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:300000-317200 Strong transcription Liver Liver
2 chr12:312400-314000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
3 chr12:312600-314000 Active TSS Brain Anterior Caudate brain
4 chr12:312600-314000 Enhancers Lung lung
5 chr12:313200-314000 Flanking Active TSS Brain Hippocampus Middle brain
6 chr12:313200-314000 Bivalent Enhancer Spleen Spleen
7 chr12:313400-314000 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr12:313400-314000 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr12:313400-314000 Enhancers Pancreas Pancrea
10 chr12:313600-314000 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
11 chr12:313600-314000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
12 chr12:313600-314600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr12:313600-314600 Enhancers Brain Angular Gyrus brain
14 chr12:313600-318200 Weak transcription Fetal Kidney kidney
15 chr12:313600-319600 Weak transcription Gastric stomach
16 chr12:313800-314000 Bivalent Enhancer H1 Cell Line embryonic stem cell
17 chr12:313800-314000 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
18 chr12:313800-314200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
19 chr12:313800-314200 Weak transcription Fetal Lung lung
20 chr12:313800-315000 Weak transcription Right Ventricle heart

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