Variant report

Variant rs16991439
Chromosome Location chr22:33270191-33270192
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33227000-33272400 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr22:33237400-33282200 Weak transcription Fetal Brain Female brain
3 chr22:33257800-33282000 Weak transcription HepG2 liver
4 chr22:33259000-33270800 Weak transcription Fetal Lung lung
5 chr22:33259400-33270200 Weak transcription Fetal Muscle Trunk muscle
6 chr22:33261200-33270400 Weak transcription H1 Cell Line embryonic stem cell
7 chr22:33265200-33282000 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr22:33265600-33287000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr22:33268600-33270800 Enhancers K562 blood
10 chr22:33269400-33272400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr22:33269400-33272400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr22:33269600-33271400 Enhancers Fetal Intestine Small intestine
13 chr22:33269600-33272200 Enhancers Fetal Thymus thymus
14 chr22:33270000-33271600 Enhancers Fetal Intestine Large intestine
15 chr22:33270000-33272400 Enhancers Primary hematopoietic stem cells blood

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