Variant report

Variant	rs614303
Chromosome Location	chr2:21313577-21313578
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs13411597	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1367119	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1367120	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1652416	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1652417	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1652419	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1652420	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1652421	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1652422	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1652423	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1712246	0.80[EUR][1000 genomes]
rs1712247	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1712248	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1712250	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1712251	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs312936	0.84[EUR][1000 genomes]
rs312944	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs312979	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs312981	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs312982	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs312983	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs312984	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs312985	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34872576	1.00[ASN][1000 genomes]
rs34916112	1.00[ASN][1000 genomes]
rs4560142	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4591370	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs473269	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs477146	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs478442	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs478588	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs483621	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs486246	0.85[EUR][1000 genomes]
rs487858	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs490757	0.85[EUR][1000 genomes]
rs492255	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs494315	0.85[EUR][1000 genomes]
rs494465	0.85[EUR][1000 genomes]
rs502323	0.85[EUR][1000 genomes]
rs503105	0.91[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs504091	0.84[EUR][1000 genomes]
rs504616	0.81[EUR][1000 genomes]
rs506585	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs507616	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs515135	0.83[EUR][1000 genomes]
rs522250	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs522822	0.85[EUR][1000 genomes]
rs522963	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs525172	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs527034	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs527259	0.80[EUR][1000 genomes]
rs529396	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs529697	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs530474	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs531380	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs532225	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs532300	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs533211	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs533772	0.82[EUR][1000 genomes]
rs540897	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs541041	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541569	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs544039	0.90[CEU][hapmap]
rs544450	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs547179	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs547235	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs548145	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs548506	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs557197	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs558130	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs558342	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs559318	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs559967	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs560408	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs560522	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs561850	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs562338	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs563290	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs563719	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs563752	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs570033	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs572246	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs573314	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs574461	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs580889	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs581411	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs668948	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs672889	1.00[ASN][1000 genomes]
rs67332771	1.00[ASN][1000 genomes]
rs9798358	0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr2:21312400-21314800	Weak transcription	HepG2	liver
2	chr2:21312800-21321000	Weak transcription	H9 Cell Line	embryonic stem cell

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