Variant report

Variant rs73369026
Chromosome Location chr21:46652238-46652239
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46637800-46668600 Weak transcription Right Atrium heart
2 chr21:46643800-46664600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr21:46648800-46654200 Weak transcription Primary T helper cells fromperipheralblood blood
4 chr21:46648800-46654600 Weak transcription Fetal Brain Male brain
5 chr21:46648800-46656400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr21:46651800-46652400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
7 chr21:46652200-46652400 Bivalent Enhancer Primary T cells fromperipheralblood blood
8 chr21:46652200-46652400 Enhancers Primary T helper cells PMA-I stimulated --
9 chr21:46652200-46652400 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
10 chr21:46652200-46652400 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
11 chr21:46652200-46652400 Enhancers Primary mononuclear cells fromperipheralblood Blood
12 chr21:46652200-46652400 Enhancers Pancreas Pancrea
13 chr21:46652200-46652800 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr21:46652200-46654800 Weak transcription Cortex derived primary cultured neurospheres brain

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