Variant report

Variant	rs72704457
Chromosome Location	chr1:179479557-179479558
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:179477575..179481033-chr1:179483963..179487085,3	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10494519	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11799973	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11801024	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11802834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11805319	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11805875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11806287	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11808359	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11809095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1854336	0.80[EUR][1000 genomes]
rs2209923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2209924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6682308	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs67908894	0.80[EUR][1000 genomes]
rs72704407	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72704408	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72704416	1.00[EUR][1000 genomes]
rs72704426	1.00[EUR][1000 genomes]
rs72704429	1.00[EUR][1000 genomes]
rs72704430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72704431	1.00[EUR][1000 genomes]
rs72704464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72704465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72704468	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72706703	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72706705	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72706706	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72706707	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72706708	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72706709	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs72717527	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs72719210	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72719259	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72721234	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72721237	0.80[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	esv1820823	chr1:179455645-179479803	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr1:179478800-179479600	Enhancers	Primary B cells from peripheral blood	blood
2	chr1:179479400-179479600	Flanking Active TSS	GM12878-XiMat	blood

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