Variant report

Variant	rs13081974
Chromosome Location	chr3:144195796-144195797
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1036439	0.84[ASN][1000 genomes]
rs10490827	0.92[ASN][1000 genomes]
rs10935507	0.90[ASN][1000 genomes]
rs12631899	0.92[ASN][1000 genomes]
rs12632855	0.91[ASN][1000 genomes]
rs12638468	0.99[ASN][1000 genomes]
rs12638544	0.96[ASN][1000 genomes]
rs12639461	0.92[ASN][1000 genomes]
rs1815189	0.83[ASN][1000 genomes]
rs4290842	0.98[ASN][1000 genomes]
rs4681126	0.93[ASN][1000 genomes]
rs56096828	0.92[ASN][1000 genomes]
rs56178175	0.97[ASN][1000 genomes]
rs56191622	0.85[ASN][1000 genomes]
rs56228220	0.92[ASN][1000 genomes]
rs57393618	0.97[ASN][1000 genomes]
rs59900584	0.91[ASN][1000 genomes]
rs61641065	0.85[ASN][1000 genomes]
rs73009099	0.98[ASN][1000 genomes]
rs73871205	0.97[ASN][1000 genomes]
rs73871207	0.97[ASN][1000 genomes]
rs73871211	0.92[ASN][1000 genomes]
rs73871221	0.91[ASN][1000 genomes]
rs73871228	0.84[ASN][1000 genomes]
rs73871240	0.81[ASN][1000 genomes]
rs73871243	0.81[ASN][1000 genomes]
rs73871244	0.81[ASN][1000 genomes]
rs73871245	0.81[ASN][1000 genomes]
rs73871248	0.81[ASN][1000 genomes]
rs73871252	0.81[ASN][1000 genomes]
rs73875119	0.98[ASN][1000 genomes]
rs73875127	0.98[ASN][1000 genomes]
rs73875134	0.98[ASN][1000 genomes]
rs73875140	0.97[ASN][1000 genomes]
rs7630402	0.92[ASN][1000 genomes]
rs7636316	0.91[ASN][1000 genomes]
rs7637942	0.93[ASN][1000 genomes]
rs920146	0.94[ASN][1000 genomes]
rs9844730	0.90[ASN][1000 genomes]
rs9866198	0.93[ASN][1000 genomes]
rs9866442	0.93[ASN][1000 genomes]
rs9873732	0.94[ASN][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	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1011685	chr3:143959237-144218424	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536751	chr3:143959237-144218424	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2756108	chr3:144177836-144301659	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv877571	chr3:144188561-144291254	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:144193800-144196200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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