Variant report

Variant	rs17022182
Chromosome Location	chr4:147895126-147895127
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POU4F2-3	chr4:147895010-147895140	XLOC_003726

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10519843	1.00[EUR][1000 genomes]
rs10519858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1370302	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1437260	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022075	1.00[EUR][1000 genomes]
rs17022229	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022275	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17022292	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28694531	1.00[EUR][1000 genomes]
rs4301138	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55789811	1.00[EUR][1000 genomes]
rs55862662	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56919404	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56939845	1.00[EUR][1000 genomes]
rs59033491	1.00[EUR][1000 genomes]
rs59895059	1.00[EUR][1000 genomes]
rs6537442	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6811983	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6813219	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6840129	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6850704	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6851748	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6857268	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73852704	1.00[EUR][1000 genomes]
rs73852707	1.00[EUR][1000 genomes]
rs73852718	1.00[EUR][1000 genomes]
rs73852721	1.00[EUR][1000 genomes]
rs73852722	1.00[EUR][1000 genomes]
rs73852734	1.00[EUR][1000 genomes]
rs73852736	1.00[EUR][1000 genomes]
rs73852787	1.00[EUR][1000 genomes]
rs73852788	1.00[EUR][1000 genomes]
rs73852789	1.00[EUR][1000 genomes]
rs73852790	1.00[EUR][1000 genomes]
rs73852791	1.00[EUR][1000 genomes]
rs73852795	1.00[EUR][1000 genomes]
rs73852796	1.00[EUR][1000 genomes]
rs73852797	1.00[EUR][1000 genomes]
rs73853259	1.00[EUR][1000 genomes]
rs73853275	1.00[EUR][1000 genomes]
rs73853277	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73853283	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73853285	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73853295	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73855102	1.00[EUR][1000 genomes]
rs73855650	1.00[EUR][1000 genomes]
rs73856354	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	esv1826357	chr4:147876484-147900981	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr4:147895000-147898400	Enhancers	Primary hematopoietic stem cells	blood

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