Variant report

Variant	rs7412448
Chromosome Location	chr1:69326982-69326983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10047054	0.82[ASN][1000 genomes]
rs10493451	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11209362	1.00[ASN][1000 genomes]
rs11209370	0.82[ASN][1000 genomes]
rs11576549	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11579356	1.00[ASN][1000 genomes]
rs11581649	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11582908	0.88[ASN][1000 genomes]
rs11801267	0.82[ASN][1000 genomes]
rs11801354	0.88[ASN][1000 genomes]
rs11801756	0.88[ASN][1000 genomes]
rs11802814	0.82[ASN][1000 genomes]
rs11804299	0.82[ASN][1000 genomes]
rs11806894	0.88[ASN][1000 genomes]
rs11809118	0.88[ASN][1000 genomes]
rs12087596	0.82[ASN][1000 genomes]
rs13375505	0.82[ASN][1000 genomes]
rs1396022	0.82[ASN][1000 genomes]
rs1507855	0.82[ASN][1000 genomes]
rs1507858	0.82[ASN][1000 genomes]
rs17435073	0.82[AMR][1000 genomes]
rs28599531	0.88[ASN][1000 genomes]
rs4301671	0.82[ASN][1000 genomes]
rs4328112	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4390220	0.82[ASN][1000 genomes]
rs4420133	0.82[ASN][1000 genomes]
rs4484966	0.82[ASN][1000 genomes]
rs4539178	0.82[ASN][1000 genomes]
rs4649904	0.82[ASN][1000 genomes]
rs55815583	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56026859	0.82[ASN][1000 genomes]
rs58102432	0.88[ASN][1000 genomes]
rs58815715	0.82[ASN][1000 genomes]
rs6658033	0.82[ASN][1000 genomes]
rs6658121	0.82[ASN][1000 genomes]
rs6658623	0.82[ASN][1000 genomes]
rs6662460	0.82[ASN][1000 genomes]
rs6662550	0.82[ASN][1000 genomes]
rs6662842	0.82[ASN][1000 genomes]
rs6673849	0.82[ASN][1000 genomes]
rs6682095	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6682255	0.82[ASN][1000 genomes]
rs72680475	0.88[ASN][1000 genomes]
rs72680481	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72680485	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72680492	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72680493	0.82[ASN][1000 genomes]
rs72680496	0.82[ASN][1000 genomes]
rs72682206	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72682210	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72682218	0.82[ASN][1000 genomes]
rs72682221	0.91[AMR][1000 genomes]
rs72682222	0.82[ASN][1000 genomes]
rs7414744	1.00[ASN][1000 genomes]
rs7547769	0.82[ASN][1000 genomes]
rs7551318	0.88[ASN][1000 genomes]
rs9436417	0.88[ASN][1000 genomes]
rs9436422	0.82[ASN][1000 genomes]
rs9436423	0.82[ASN][1000 genomes]
rs9436863	0.82[ASN][1000 genomes]
rs9436866	0.82[ASN][1000 genomes]
rs9803974	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9804111	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs994176	0.82[ASN][1000 genomes]
rs9988609	1.00[ASN][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	nsv871131	chr1:69323222-69427276	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69324800-69327000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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