Variant report

Variant rs5992515
Chromosome Location chr22:20147392-20147393
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:20120600-20149600 Weak transcription H9 Cell Line embryonic stem cell
2 chr22:20133400-20149600 Weak transcription Esophagus oesophagus
3 chr22:20135000-20149800 Weak transcription Pancreas Pancrea
4 chr22:20142800-20149400 Enhancers Primary hematopoietic stem cells blood
5 chr22:20143000-20147400 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr22:20144200-20148000 Strong transcription Right Atrium heart
7 chr22:20144800-20147600 Enhancers Fetal Thymus thymus
8 chr22:20145000-20149400 Weak transcription Spleen Spleen
9 chr22:20145600-20147800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr22:20145800-20147400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr22:20145800-20147800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr22:20146800-20148000 Enhancers Brain Germinal Matrix brain
13 chr22:20147200-20147400 Enhancers Fetal Brain Male brain
14 chr22:20147200-20147600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr22:20147200-20149400 Enhancers Primary hematopoietic stem cells short term culture blood

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