Variant report

Variant rs1902906
Chromosome Location chr12:41858545-41858546
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:41829600-41860600 Weak transcription Aorta Aorta
2 chr12:41848600-41860800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr12:41853400-41860200 Weak transcription Brain Germinal Matrix brain
4 chr12:41853800-41859200 Weak transcription Fetal Lung lung
5 chr12:41855000-41859400 Weak transcription Brain Cingulate Gyrus brain
6 chr12:41855000-41860600 Weak transcription Brain Inferior Temporal Lobe brain
7 chr12:41855000-41861000 Weak transcription Brain Anterior Caudate brain
8 chr12:41855200-41859400 Weak transcription Brain Substantia Nigra brain
9 chr12:41855400-41858800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr12:41855400-41860600 Weak transcription Brain Hippocampus Middle brain
11 chr12:41856400-41859000 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr12:41857600-41860200 Enhancers Colon Smooth Muscle Colon
13 chr12:41858000-41858800 Weak transcription Stomach Smooth Muscle stomach
14 chr12:41858000-41859400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr12:41858400-41858800 Enhancers HUES64 Cell Line embryonic stem cell
16 chr12:41858400-41863000 Enhancers iPS-20b Cell Line embryonic stem cell

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