Variant report

Variant rs6934027
Chromosome Location chr6:11900906-11900907
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11900400-11901000 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr6:11900400-11901600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr6:11900400-11901600 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr6:11900600-11901000 Enhancers HUES64 Cell Line embryonic stem cell
5 chr6:11900600-11901200 Weak transcription H1 Cell Line embryonic stem cell
6 chr6:11900800-11901000 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
7 chr6:11900800-11901200 Enhancers HUES6 Cell Line embryonic stem cell
8 chr6:11900800-11901200 Enhancers Primary T cells from cord blood blood
9 chr6:11900800-11901400 Enhancers Primary T helper naive cells fromperipheralblood blood
10 chr6:11900800-11901600 Flanking Active TSS HUES48 Cell Line embryonic stem cell
11 chr6:11900800-11902000 Enhancers Primary T helper cells fromperipheralblood blood
12 chr6:11900800-11902200 Enhancers Primary T regulatory cells fromperipheralblood blood

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