Variant report

Variant	rs73426941
Chromosome Location	chr9:18250768-18250769
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10810959	1.00[AMR][1000 genomes]
rs1329723	1.00[AMR][1000 genomes]
rs1411152	1.00[AMR][1000 genomes]
rs1417038	1.00[AMR][1000 genomes]
rs1854548	1.00[AMR][1000 genomes]
rs2265843	1.00[AMR][1000 genomes]
rs2265962	1.00[AMR][1000 genomes]
rs2493745	1.00[AMR][1000 genomes]
rs2493746	1.00[AMR][1000 genomes]
rs2585579	1.00[AMR][1000 genomes]
rs2791444	1.00[AMR][1000 genomes]
rs2809855	1.00[AMR][1000 genomes]
rs2819202	1.00[AMR][1000 genomes]
rs56137310	1.00[AMR][1000 genomes]
rs57035045	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58927234	1.00[AMR][1000 genomes]
rs59895508	1.00[AMR][1000 genomes]
rs61086890	1.00[AMR][1000 genomes]
rs7028195	1.00[AMR][1000 genomes]
rs73420855	1.00[AMR][1000 genomes]
rs73420856	1.00[AMR][1000 genomes]
rs73420860	1.00[AMR][1000 genomes]
rs73420864	1.00[AMR][1000 genomes]
rs73420866	1.00[AMR][1000 genomes]
rs73420869	1.00[AMR][1000 genomes]
rs73420873	1.00[AMR][1000 genomes]
rs73422913	1.00[AMR][1000 genomes]
rs73424909	1.00[AMR][1000 genomes]
rs73424911	1.00[AMR][1000 genomes]
rs73426948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9407898	1.00[AMR][1000 genomes]
rs9407901	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021605	chr9:18002205-18271109	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv892680	chr9:18089614-18267185	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892682	chr9:18166112-18272700	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv831522	chr9:18231982-18459492	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	esv2764161	chr9:18247433-18443060	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr9:18225800-18260600	Weak transcription	Aorta	Aorta
2	chr9:18250200-18250800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr9:18250200-18250800	Enhancers	NHDF-Ad	bronchial
4	chr9:18250400-18250800	Enhancers	NHEK	skin
5	chr9:18250600-18255400	Weak transcription	Fetal Heart	heart
6	chr9:18250600-18255400	Weak transcription	Osteobl	bone
7	chr9:18250600-18255800	Weak transcription	NH-A	brain

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