Variant report

Variant rs10176529
Chromosome Location chr2:50992650-50992651
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50983200-50996800 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr2:50991400-50993400 Enhancers Pancreatic Islets Pancreatic Islet
3 chr2:50991800-50993000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:50991800-50993400 Enhancers Brain Cingulate Gyrus brain
5 chr2:50991800-50997000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:50992000-50993000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr2:50992000-50993000 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr2:50992200-50992800 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr2:50992200-50992800 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:50992200-50993400 Enhancers Fetal Kidney kidney
11 chr2:50992400-50993000 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr2:50992600-50992800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr2:50992600-50993000 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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