Variant report

Variant rs12797437
Chromosome Location chr11:108992236-108992237
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:108990400-108992600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
2 chr11:108990400-108994800 Enhancers Fetal Heart heart
3 chr11:108990600-108992800 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr11:108990800-108992600 Enhancers HUES64 Cell Line embryonic stem cell
5 chr11:108990800-108993000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr11:108991000-108992600 Enhancers H9 Cell Line embryonic stem cell
7 chr11:108991000-108992600 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr11:108991200-108992600 Enhancers H1 Cell Line embryonic stem cell
9 chr11:108991200-108992600 Enhancers HUES6 Cell Line embryonic stem cell
10 chr11:108991200-108992800 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr11:108991400-108994600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr11:108991600-108994400 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr11:108992000-108992400 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr11:108992200-108992400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr11:108992200-108992400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr11:108992200-108992600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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