Variant report

Variant rs9979329
Chromosome Location chr21:48036209-48036210
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:48025800-48054800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr21:48026600-48040000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr21:48026800-48040000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr21:48030800-48039000 Weak transcription Primary T killer memory cells from peripheral blood blood
5 chr21:48031000-48039800 Weak transcription HepG2 liver
6 chr21:48031000-48040000 Weak transcription Primary T cells fromperipheralblood blood
7 chr21:48031000-48040000 Weak transcription Primary T helper naive cells from peripheral blood blood
8 chr21:48034600-48039000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr21:48036000-48037400 Enhancers Primary T helper naive cells fromperipheralblood blood
10 chr21:48036000-48037600 Enhancers Primary T cells from cord blood blood
11 chr21:48036000-48037600 Enhancers Primary T killer naive cells fromperipheralblood blood

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