Variant report

Variant	rs1175123
Chromosome Location	chr1:192240064-192240065
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:192230860..192232760-chr1:192239586..192242389,2	K562	blood:
2	chr1:192238542..192241818-chr1:192250028..192252934,3	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10157255	0.95[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap]
rs10494672	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10801111	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10921129	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10921133	0.87[CEU][hapmap];0.92[JPT][hapmap]
rs1124172	0.91[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap]
rs1175121	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1175126	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1175127	0.81[AMR][1000 genomes]
rs1175128	0.81[AMR][1000 genomes]
rs1175129	0.82[AMR][1000 genomes]
rs1175132	0.80[AMR][1000 genomes]
rs1175139	0.96[CEU][hapmap]
rs1175142	0.92[CHB][hapmap]
rs1175145	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs1175147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1175148	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1175152	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1175154	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1175155	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1175156	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1175158	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1177797	0.82[AMR][1000 genomes]
rs12124127	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs12564406	0.93[CHB][hapmap]
rs12566011	0.93[CHB][hapmap]
rs12567011	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1339129	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1339130	0.93[CHB][hapmap]
rs1339131	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs1339132	0.93[CHB][hapmap]
rs1416500	0.92[CHB][hapmap]
rs1572729	0.91[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap]
rs17413409	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1892146	0.84[CEU][hapmap];0.92[JPT][hapmap]
rs1934087	0.92[CHB][hapmap]
rs2211111	0.92[CHB][hapmap]
rs2369658	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6428094	0.95[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6428095	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6659110	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6659966	0.93[CHB][hapmap]
rs6663865	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6684918	0.93[CHB][hapmap]
rs72732935	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7519610	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7528947	0.91[CEU][hapmap];0.92[JPT][hapmap]
rs7532216	0.95[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7538387	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7544311	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7545041	0.93[CHB][hapmap]
rs7545796	0.93[CHB][hapmap]
rs7554467	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7554535	0.88[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs946421	0.95[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap]

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	nsv548649	chr1:192215064-192378979	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv872829	chr1:192230089-192370110	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv872830	chr1:192236376-192353005	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192236600-192241800	Weak transcription	K562	blood
2	chr1:192239200-192240400	Enhancers	HUVEC	blood vessel
3	chr1:192239800-192240200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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