Variant report

Variant rs6726061
Chromosome Location chr2:210449349-210449350
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210443600-210461000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:210444800-210456800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr2:210445400-210449600 Weak transcription iPS-20b Cell Line embryonic stem cell
4 chr2:210446200-210456800 Weak transcription Brain Anterior Caudate brain
5 chr2:210446600-210461600 Weak transcription Brain Angular Gyrus brain
6 chr2:210446800-210449400 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr2:210447800-210460400 Weak transcription Brain Inferior Temporal Lobe brain
8 chr2:210448000-210449800 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr2:210448200-210449600 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr2:210448600-210452000 Enhancers Fetal Brain Male brain
11 chr2:210448800-210449600 Enhancers Brain Cingulate Gyrus brain
12 chr2:210448800-210450400 Enhancers Cortex derived primary cultured neurospheres brain
13 chr2:210449000-210449600 Genic enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr2:210449000-210449600 Enhancers Fetal Brain Female brain
15 chr2:210449000-210451200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr2:210449200-210451000 Weak transcription Brain Germinal Matrix brain

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