Variant report

Variant rs8138714
Chromosome Location chr22:20149170-20149171
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr22:20145000-20149400 Weak transcription Spleen Spleen
6 chr22:20147200-20149400 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr22:20147400-20149600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr22:20147800-20149600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr22:20147800-20149600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr22:20147800-20152600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr22:20148800-20149800 Bivalent Enhancer Placenta Placenta
12 chr22:20149000-20149200 Enhancers Fetal Thymus thymus
13 chr22:20149000-20149400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr22:20149000-20150000 Strong transcription Right Atrium heart

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