Variant report

Variant rs78961361
Chromosome Location chr19:53267419-53267420
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:53262000-53268600 Weak transcription HUES64 Cell Line embryonic stem cell
2 chr19:53262000-53269000 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr19:53262200-53268800 Weak transcription Dnd41 blood
4 chr19:53263200-53267800 Enhancers Placenta Placenta
5 chr19:53263200-53268800 Weak transcription H9 Cell Line embryonic stem cell
6 chr19:53264600-53285200 ZNF genes & repeats Liver Liver
7 chr19:53265600-53272200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr19:53265600-53282400 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
9 chr19:53267000-53269200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr19:53267000-53272600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr19:53267200-53271800 Weak transcription Fetal Stomach stomach
12 chr19:53267200-53273600 ZNF genes & repeats Adipose Nuclei Adipose
13 chr19:53267400-53268000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr19:53267400-53268400 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell

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