Variant report

Variant rs3768830
Chromosome Location chr2:210533416-210533417
allele A/C
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 chr2:210528600-210534000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr2:210528600-210550200 Weak transcription Brain Substantia Nigra brain
4 chr2:210528800-210533800 Weak transcription Brain Anterior Caudate brain
5 chr2:210528800-210550200 Weak transcription Brain Inferior Temporal Lobe brain
6 chr2:210530400-210536000 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr2:210531200-210533800 Weak transcription Fetal Brain Male brain
8 chr2:210531200-210535400 Weak transcription Fetal Brain Female brain
9 chr2:210531400-210533800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr2:210531400-210534600 Weak transcription Brain Germinal Matrix brain
11 chr2:210531400-210535800 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr2:210531400-210587800 Weak transcription Brain Angular Gyrus brain
13 chr2:210532400-210535400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr2:210532400-210537000 Enhancers Cortex derived primary cultured neurospheres brain
15 chr2:210532800-210535000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr2:210532800-210535600 Weak transcription HUES64 Cell Line embryonic stem cell
17 chr2:210532800-210536000 Weak transcription iPS-20b Cell Line embryonic stem cell

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