Variant report

Variant rs11169904
Chromosome Location chr12:37998914-37998915
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:37989800-38041200 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
2 chr12:37990000-38040800 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
3 chr12:37990400-38014000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr12:37995200-38003400 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
5 chr12:37997200-38000200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
6 chr12:37997800-38000200 ZNF genes & repeats HepG2 liver
7 chr12:37998000-38002400 ZNF genes & repeats Primary T cells from cord blood blood
8 chr12:37998000-38002800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
9 chr12:37998200-38000000 ZNF genes & repeats hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr12:37998400-37999200 Weak transcription Brain Cingulate Gyrus brain
11 chr12:37998400-37999400 Weak transcription Brain Substantia Nigra brain

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