Variant report

Variant rs367799012
Chromosome Location chr14:19006940-19006941
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:19000400-19017400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr14:19000600-19012800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
3 chr14:19000600-19017200 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
4 chr14:19000600-19017800 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
5 chr14:19000600-19020200 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
6 chr14:19003400-19007000 ZNF genes & repeats hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr14:19004200-19011400 Weak transcription Aorta Aorta
8 chr14:19004200-19016200 Weak transcription K562 blood
9 chr14:19005200-19008800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
10 chr14:19005800-19007200 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
11 chr14:19006600-19011400 Weak transcription Primary T helper naive cells from peripheral blood blood
12 chr14:19006600-19011400 Weak transcription Colon Smooth Muscle Colon

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