Variant report

Variant rs1446598
Chromosome Location chr2:210253983-210253984
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210248800-210256000 Weak transcription NHLF lung
2 chr2:210251400-210254000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:210253000-210254600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:210253000-210254800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr2:210253400-210254000 Enhancers Placenta Amnion Placenta Amnion
6 chr2:210253600-210254000 Flanking Active TSS Fetal Brain Female brain
7 chr2:210253600-210254400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr2:210253600-210254400 Enhancers Cortex derived primary cultured neurospheres brain
9 chr2:210253800-210254000 Active TSS Fetal Brain Male brain
10 chr2:210253800-210254400 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:210253800-210254600 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr2:210253800-210254600 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain

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