Variant report

Variant rs3768826
Chromosome Location chr2:210536328-210536329
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210518200-210543200 Weak transcription Aorta Aorta
2 chr2:210528600-210550200 Weak transcription Brain Substantia Nigra brain
3 chr2:210528800-210550200 Weak transcription Brain Inferior Temporal Lobe brain
4 chr2:210531400-210587800 Weak transcription Brain Angular Gyrus brain
5 chr2:210532400-210537000 Enhancers Cortex derived primary cultured neurospheres brain
6 chr2:210533800-210537600 Enhancers Fetal Brain Male brain
7 chr2:210535000-210536400 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr2:210535000-210536600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr2:210535000-210537000 Genic enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr2:210535400-210537000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
11 chr2:210535400-210537000 Enhancers Brain Hippocampus Middle brain
12 chr2:210535800-210536600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr2:210535800-210537000 Enhancers Brain Anterior Caudate brain
14 chr2:210536000-210536400 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr2:210536000-210536400 Active TSS Fetal Brain Female brain
16 chr2:210536200-210536600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
17 chr2:210536200-210537600 Enhancers Brain Germinal Matrix brain

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