Variant report

Variant rs201084958
Chromosome Location chr16:35228619-35228620
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:35216200-35229000 Weak transcription Primary T helper naive cells from peripheral blood blood
2 chr16:35216200-35229000 Weak transcription Ovary ovary
3 chr16:35219000-35229000 Weak transcription Small Intestine intestine
4 chr16:35220800-35229000 Weak transcription Primary T killer memory cells from peripheral blood blood
5 chr16:35220800-35229000 Weak transcription Aorta Aorta
6 chr16:35220800-35229000 Weak transcription NH-A brain
7 chr16:35220800-35229000 Weak transcription NHLF lung
8 chr16:35224400-35237800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr16:35224600-35243000 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
10 chr16:35225200-35229000 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr16:35226600-35229600 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
12 chr16:35227000-35229000 Weak transcription Right Ventricle heart
13 chr16:35227400-35242800 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
14 chr16:35227600-35229000 Weak transcription Fetal Heart heart
15 chr16:35227800-35229000 Weak transcription Liver Liver
16 chr16:35228600-35229600 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
17 chr16:35228600-35229600 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell

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