Variant report

Variant	rs16945922
Chromosome Location	chr16:48223792-48223793
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs16945857	1.00[AMR][1000 genomes]
rs16945864	1.00[AMR][1000 genomes]
rs16945867	1.00[AMR][1000 genomes]
rs16945872	1.00[AMR][1000 genomes]
rs16945876	1.00[AMR][1000 genomes]
rs16945878	1.00[AMR][1000 genomes]
rs16945880	1.00[AMR][1000 genomes]
rs16945881	1.00[AMR][1000 genomes]
rs16945883	1.00[AMR][1000 genomes]
rs16945890	1.00[AMR][1000 genomes]
rs16945892	1.00[AMR][1000 genomes]
rs16945895	1.00[AMR][1000 genomes]
rs16945897	1.00[AMR][1000 genomes]
rs16945901	1.00[AMR][1000 genomes]
rs16945903	1.00[AMR][1000 genomes]
rs16945904	1.00[AMR][1000 genomes]
rs16945926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16945943	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16945946	1.00[AMR][1000 genomes]
rs17815694	1.00[AMR][1000 genomes]
rs55913020	1.00[AMR][1000 genomes]
rs58041814	1.00[AMR][1000 genomes]
rs59000493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59404336	1.00[AMR][1000 genomes]
rs59546442	1.00[AMR][1000 genomes]
rs59815620	1.00[AMR][1000 genomes]
rs60438421	1.00[AMR][1000 genomes]
rs60752576	1.00[AMR][1000 genomes]
rs61695297	1.00[AMR][1000 genomes]
rs7184973	1.00[AMR][1000 genomes]
rs7187621	1.00[AMR][1000 genomes]
rs7197710	1.00[AMR][1000 genomes]
rs7204946	1.00[AMR][1000 genomes]
rs74018257	1.00[AMR][1000 genomes]
rs74018258	1.00[AMR][1000 genomes]
rs74018260	1.00[AMR][1000 genomes]
rs74018262	1.00[AMR][1000 genomes]
rs74018265	1.00[AMR][1000 genomes]
rs74018274	1.00[AMR][1000 genomes]
rs74018275	1.00[AMR][1000 genomes]
rs74018276	1.00[AMR][1000 genomes]
rs74018277	1.00[AMR][1000 genomes]
rs74018278	1.00[AMR][1000 genomes]
rs74018281	1.00[AMR][1000 genomes]
rs74018285	1.00[AMR][1000 genomes]
rs74018286	1.00[AMR][1000 genomes]
rs74018287	1.00[AMR][1000 genomes]
rs74018289	1.00[AMR][1000 genomes]
rs74018292	1.00[AMR][1000 genomes]
rs74018293	1.00[AMR][1000 genomes]
rs74018294	1.00[AMR][1000 genomes]
rs74018296	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1059259	chr16:48113396-48304404	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv542916	chr16:48113396-48304404	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48199200-48226600	Weak transcription	Spleen	Spleen
2	chr16:48216400-48226400	Weak transcription	Esophagus	oesophagus
3	chr16:48218800-48228000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr16:48220800-48224000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr16:48221600-48224000	Enhancers	HepG2	liver
6	chr16:48222600-48224000	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr16:48223400-48223800	Enhancers	Monocytes-CD14+_RO01746	blood

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