Variant report

Variant rs17041013
Chromosome Location chr2:50976615-50976616
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50972200-50978200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr2:50974400-50978200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr2:50975000-50976800 Enhancers Fetal Brain Female brain
4 chr2:50975200-50977200 Enhancers Cortex derived primary cultured neurospheres brain
5 chr2:50975800-50977000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:50975800-50978400 Weak transcription Fetal Brain Male brain
7 chr2:50976000-50977200 Enhancers Brain Cingulate Gyrus brain
8 chr2:50976000-50978000 Weak transcription Psoas Muscle Psoas
9 chr2:50976000-50978600 Weak transcription Fetal Muscle Leg muscle
10 chr2:50976200-50976800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr2:50976200-50977400 Enhancers Brain Hippocampus Middle brain
12 chr2:50976200-50978200 Weak transcription Brain Germinal Matrix brain
13 chr2:50976200-50982800 Weak transcription Brain Substantia Nigra brain
14 chr2:50976600-50979800 Enhancers Fetal Stomach stomach
15 chr2:50976600-50983200 Weak transcription Brain Inferior Temporal Lobe brain

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