Variant report

Variant rs77024719
Chromosome Location chr19:21380878-21380879
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:21370000-21382200 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr19:21370200-21381000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr19:21373200-21381800 Weak transcription Dnd41 blood
4 chr19:21377800-21381800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr19:21378000-21381200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr19:21379200-21382400 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr19:21380000-21381200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr19:21380200-21381800 Enhancers Primary neutrophils fromperipheralblood blood
9 chr19:21380400-21381200 Enhancers Placenta Amnion Placenta Amnion
10 chr19:21380400-21382200 Enhancers K562 blood
11 chr19:21380600-21389600 Enhancers Ovary ovary
12 chr19:21380800-21381000 Enhancers Placenta Placenta
13 chr19:21380800-21382000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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