Variant report

Variant	rs12742451
Chromosome Location	chr1:158395176-158395177
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs1006223	0.80[EUR][1000 genomes]
rs10489829	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10489830	1.00[ASN][1000 genomes]
rs10908649	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1119029	0.99[ASN][1000 genomes]
rs11264971	0.97[ASN][1000 genomes]
rs12118413	0.97[ASN][1000 genomes]
rs12119297	0.99[ASN][1000 genomes]
rs12122595	0.97[ASN][1000 genomes]
rs12125990	0.97[ASN][1000 genomes]
rs12127971	0.97[ASN][1000 genomes]
rs12129036	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12131763	0.93[ASN][1000 genomes]
rs12132792	1.00[ASN][1000 genomes]
rs12133777	0.99[ASN][1000 genomes]
rs12134692	0.99[ASN][1000 genomes]
rs12136746	0.99[ASN][1000 genomes]
rs12136971	0.99[ASN][1000 genomes]
rs12138872	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12139611	0.99[ASN][1000 genomes]
rs12141446	0.99[ASN][1000 genomes]
rs12141449	0.99[ASN][1000 genomes]
rs12142715	0.97[ASN][1000 genomes]
rs12143038	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12144696	0.99[ASN][1000 genomes]
rs12145637	0.99[ASN][1000 genomes]
rs12239443	1.00[ASN][1000 genomes]
rs12725399	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12725721	1.00[ASN][1000 genomes]
rs12728815	0.97[ASN][1000 genomes]
rs12729052	0.97[ASN][1000 genomes]
rs12738597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12743143	1.00[ASN][1000 genomes]
rs12743313	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12744495	0.97[ASN][1000 genomes]
rs12747451	0.98[ASN][1000 genomes]
rs1321647	0.98[ASN][1000 genomes]
rs13375849	0.99[ASN][1000 genomes]
rs13376086	0.97[ASN][1000 genomes]
rs1342937	0.99[ASN][1000 genomes]
rs1342938	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1342939	0.99[ASN][1000 genomes]
rs1342940	0.99[ASN][1000 genomes]
rs1342941	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1342942	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1388267	0.97[ASN][1000 genomes]
rs1418841	0.99[ASN][1000 genomes]
rs1546064	0.99[ASN][1000 genomes]
rs1578759	0.99[ASN][1000 genomes]
rs1578760	0.99[ASN][1000 genomes]
rs17627697	0.97[ASN][1000 genomes]
rs17627858	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17628151	1.00[ASN][1000 genomes]
rs17628749	0.97[ASN][1000 genomes]
rs17678931	0.97[ASN][1000 genomes]
rs17679007	0.98[ASN][1000 genomes]
rs1907467	0.99[ASN][1000 genomes]
rs2106084	0.84[ASN][1000 genomes]
rs2188102	0.98[ASN][1000 genomes]
rs2188107	1.00[ASN][1000 genomes]
rs2188108	1.00[ASN][1000 genomes]
rs2201059	0.99[ASN][1000 genomes]
rs2213946	0.97[ASN][1000 genomes]
rs2220630	0.97[ASN][1000 genomes]
rs34199939	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34246317	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34443037	0.95[ASN][1000 genomes]
rs34616883	1.00[ASN][1000 genomes]
rs34959155	0.97[ASN][1000 genomes]
rs35053382	0.97[ASN][1000 genomes]
rs35321102	1.00[ASN][1000 genomes]
rs35358362	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35430171	0.97[ASN][1000 genomes]
rs35504011	0.97[ASN][1000 genomes]
rs35963645	0.97[ASN][1000 genomes]
rs4628505	0.99[ASN][1000 genomes]
rs4644490	0.99[ASN][1000 genomes]
rs4656284	0.97[ASN][1000 genomes]
rs4656286	0.98[ASN][1000 genomes]
rs56125590	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56937999	0.97[ASN][1000 genomes]
rs57472964	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57525598	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58605957	1.00[ASN][1000 genomes]
rs59524892	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59542663	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60351230	0.99[ASN][1000 genomes]
rs61034754	0.99[ASN][1000 genomes]
rs6427437	0.97[ASN][1000 genomes]
rs6660236	0.99[ASN][1000 genomes]
rs6672590	0.99[ASN][1000 genomes]
rs6675399	0.99[ASN][1000 genomes]
rs6692530	0.97[ASN][1000 genomes]
rs66946798	0.99[ASN][1000 genomes]
rs6699757	0.97[ASN][1000 genomes]
rs67317531	0.97[ASN][1000 genomes]
rs7418542	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7525550	1.00[ASN][1000 genomes]
rs7540866	0.99[ASN][1000 genomes]
rs961562	0.97[ASN][1000 genomes]
rs977384	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs989203	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv998569	chr1:158317392-158443389	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158394000-158396200	Enhancers	Dnd41	blood
2	chr1:158394800-158395200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:158394800-158396000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr1:158395000-158395200	Flanking Active TSS	Thymus	Thymus
5	chr1:158395000-158395400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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