Variant report

Variant rs143295539
Chromosome Location chr19:53267818-53267819
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr19:53263200-53268800 Weak transcription H9 Cell Line embryonic stem cell
5 chr19:53264600-53285200 ZNF genes & repeats Liver Liver
6 chr19:53265600-53272200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr19:53265600-53282400 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
8 chr19:53267000-53269200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr19:53267000-53272600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr19:53267200-53271800 Weak transcription Fetal Stomach stomach
11 chr19:53267200-53273600 ZNF genes & repeats Adipose Nuclei Adipose
12 chr19:53267400-53268000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr19:53267400-53268400 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
14 chr19:53267800-53268800 Weak transcription Placenta Placenta
15 chr19:53267800-53269400 Weak transcription Placenta Amnion Placenta Amnion
16 chr19:53267800-53272000 ZNF genes & repeats Primary T cells from cord blood blood

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