Variant report

Variant	rs10441039
Chromosome Location	chr7:18921122-18921123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10228341	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10235695	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10247184	1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs10252839	1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10253169	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10266268	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10268296	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10268558	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10277107	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10281987	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10282165	0.87[EUR][1000 genomes]
rs10441036	0.87[EUR][1000 genomes]
rs10486312	1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12056184	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs12056282	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs12113191	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699997	0.87[EUR][1000 genomes]
rs12700005	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12700006	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12700009	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12700011	0.87[EUR][1000 genomes]
rs12700012	0.87[EUR][1000 genomes]
rs13221164	1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13224263	0.87[EUR][1000 genomes]
rs13224833	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13230142	1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs13235810	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13237090	1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs13238702	0.87[EUR][1000 genomes]
rs13239170	0.87[EUR][1000 genomes]
rs13241140	1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13438582	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16872130	0.87[EUR][1000 genomes]
rs17140086	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs17140133	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs17140138	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs17140149	0.87[EUR][1000 genomes]
rs17140158	0.87[EUR][1000 genomes]
rs17140170	0.87[EUR][1000 genomes]
rs17140193	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17140198	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17140227	0.87[EUR][1000 genomes]
rs34018423	0.87[EUR][1000 genomes]
rs34098679	0.87[EUR][1000 genomes]
rs34302776	0.87[EUR][1000 genomes]
rs34707237	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34790980	0.87[EUR][1000 genomes]
rs34896059	0.87[EUR][1000 genomes]
rs35024729	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35057182	0.87[EUR][1000 genomes]
rs35074349	0.87[EUR][1000 genomes]
rs35334608	0.87[EUR][1000 genomes]
rs35692319	0.87[EUR][1000 genomes]
rs35936891	0.81[ASN][1000 genomes]
rs3852253	0.90[JPT][hapmap]
rs3852255	0.81[CHB][hapmap]
rs4445123	1.00[TSI][hapmap];0.87[EUR][1000 genomes]
rs55885016	0.83[ASN][1000 genomes]
rs55930836	0.81[ASN][1000 genomes]
rs59593404	0.97[ASN][1000 genomes]
rs59618106	0.94[ASN][1000 genomes]
rs6978417	0.82[ASN][1000 genomes]
rs71524253	0.87[EUR][1000 genomes]
rs71524257	0.87[EUR][1000 genomes]
rs7789261	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7808375	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7809412	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7811828	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv523497	chr7:18896011-18959381	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2756248	chr7:18911960-18977760	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1030062	chr7:18915874-18943409	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
2	chr7:18906200-18929200	Weak transcription	Left Ventricle	heart

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