Variant report

Variant	rs10770719
Chromosome Location	chr12:20906708-20906709
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10444412	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10770714	0.81[EUR][1000 genomes]
rs10770715	0.81[EUR][1000 genomes]
rs10770717	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10770718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10841604	0.81[EUR][1000 genomes]
rs10841605	0.81[EUR][1000 genomes]
rs10841606	0.80[EUR][1000 genomes]
rs10841607	0.81[EUR][1000 genomes]
rs10841608	0.81[EUR][1000 genomes]
rs10841609	0.81[EUR][1000 genomes]
rs10841610	0.81[EUR][1000 genomes]
rs10841611	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10841612	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10841613	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10841615	0.82[EUR][1000 genomes]
rs10841616	0.82[EUR][1000 genomes]
rs11045426	0.81[EUR][1000 genomes]
rs11045428	0.81[EUR][1000 genomes]
rs11045429	0.81[EUR][1000 genomes]
rs11045430	0.81[EUR][1000 genomes]
rs11045432	0.81[EUR][1000 genomes]
rs11045434	0.81[EUR][1000 genomes]
rs11045435	0.81[EUR][1000 genomes]
rs11045437	0.81[EUR][1000 genomes]
rs11045439	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11045440	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11045441	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11045446	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11045447	0.82[EUR][1000 genomes]
rs11045448	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11045452	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11045453	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11519052	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12368368	0.81[EUR][1000 genomes]
rs12368841	0.81[EUR][1000 genomes]
rs12371796	0.81[EUR][1000 genomes]
rs12371798	0.81[EUR][1000 genomes]
rs12423310	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12425904	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12810927	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12818525	0.81[EUR][1000 genomes]
rs12819311	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12821686	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1399940	0.81[EUR][1000 genomes]
rs1515765	0.81[EUR][1000 genomes]
rs1554146	0.81[EUR][1000 genomes]
rs1554147	0.81[EUR][1000 genomes]
rs1554148	0.81[EUR][1000 genomes]
rs1554149	0.80[EUR][1000 genomes]
rs1554151	0.81[EUR][1000 genomes]
rs1554152	0.81[EUR][1000 genomes]
rs1554153	0.81[EUR][1000 genomes]
rs17326431	0.81[EUR][1000 genomes]
rs17326468	0.81[EUR][1000 genomes]
rs1829003	0.81[EUR][1000 genomes]
rs2138332	0.81[EUR][1000 genomes]
rs2271656	0.81[EUR][1000 genomes]
rs2417863	0.81[EUR][1000 genomes]
rs2417864	0.81[EUR][1000 genomes]
rs35962288	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4293173	0.81[EUR][1000 genomes]
rs4360745	0.82[AFR][1000 genomes]
rs4411320	0.82[AFR][1000 genomes]
rs4468396	0.81[EUR][1000 genomes]
rs4531518	0.81[EUR][1000 genomes]
rs4581503	0.81[EUR][1000 genomes]
rs4762670	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4762772	0.81[EUR][1000 genomes]
rs4762773	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4762774	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4762777	0.94[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4762778	0.84[AFR][1000 genomes]
rs56767862	0.80[EUR][1000 genomes]
rs6487137	0.81[EUR][1000 genomes]
rs6487138	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7137980	0.80[EUR][1000 genomes]
rs7311073	0.81[EUR][1000 genomes]
rs7311098	0.81[EUR][1000 genomes]
rs7311533	0.81[EUR][1000 genomes]
rs7967660	0.82[EUR][1000 genomes]
rs7969555	0.81[EUR][1000 genomes]
rs7980844	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs953001	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs953002	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs957164	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs972505	0.81[EUR][1000 genomes]
rs972506	0.81[EUR][1000 genomes]
rs972507	0.81[EUR][1000 genomes]
rs974039	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs974040	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs974041	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043890	chr12:20659151-21309993	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv541410	chr12:20659151-21309993	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1054997	chr12:20682009-21292602	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv3391629	chr12:20866256-20908722	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1039951	chr12:20880417-20941238	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv17347	chr12:20892854-21029179	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1051454	chr12:20893994-20999635	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 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	chr12:20892800-20922200	Weak transcription	Aorta	Aorta

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