Variant report

Variant rs9392537
Chromosome Location chr6:448953-448954
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:443200-449000 Enhancers Primary T cells from cord blood blood
2 chr6:443200-453200 Weak transcription Right Atrium heart
3 chr6:444400-449400 Enhancers Primary T killer naive cells fromperipheralblood blood
4 chr6:447200-449000 Enhancers Primary T helper naive cells fromperipheralblood blood
5 chr6:447400-449000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr6:448000-452600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr6:448200-449000 Enhancers Primary T helper memory cells from peripheral blood 1 blood
8 chr6:448200-449600 Enhancers Primary T cells fromperipheralblood blood
9 chr6:448400-450400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
10 chr6:448600-449200 Enhancers Primary T helper cells PMA-I stimulated --
11 chr6:448600-449400 Enhancers Primary T helper 17 cells PMA-I stimulated --
12 chr6:448800-449800 Strong transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr6:448800-450000 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell

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