Variant report

Variant rs3768827
Chromosome Location chr2:210535419-210535420
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr2:210530400-210536000 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr2:210531400-210535800 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr2:210531400-210587800 Weak transcription Brain Angular Gyrus brain
7 chr2:210532400-210537000 Enhancers Cortex derived primary cultured neurospheres brain
8 chr2:210532800-210535600 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr2:210532800-210536000 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr2:210533800-210537600 Enhancers Fetal Brain Male brain
11 chr2:210534600-210535800 Weak transcription Brain Anterior Caudate brain
12 chr2:210534600-210535800 Enhancers Brain Germinal Matrix brain
13 chr2:210535000-210536400 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr2:210535000-210536600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr2:210535000-210537000 Genic enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr2:210535400-210536000 Enhancers Fetal Brain Female brain
17 chr2:210535400-210537000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
18 chr2:210535400-210537000 Enhancers Brain Hippocampus Middle brain

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