Variant report

Variant rs113344559
Chromosome Location chr19:22263333-22263334
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:22235800-22270400 Weak transcription Primary T helper naive cells from peripheral blood blood
2 chr19:22253200-22272400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr19:22258800-22265200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
4 chr19:22260000-22264400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr19:22261000-22264200 Weak transcription Fetal Intestine Large intestine
6 chr19:22261400-22263400 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr19:22261800-22263400 ZNF genes & repeats Primary hematopoietic stem cells blood
8 chr19:22261800-22266200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
9 chr19:22262000-22263400 ZNF genes & repeats Primary T helper cells fromperipheralblood blood
10 chr19:22262000-22263400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr19:22262200-22263400 ZNF genes & repeats Primary B cells from cord blood blood
12 chr19:22262200-22263400 Strong transcription Pancreas Pancrea
13 chr19:22263000-22263400 ZNF genes & repeats Aorta Aorta
14 chr19:22263200-22267600 Weak transcription Ovary ovary

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