Variant report

Variant	rs11957251
Chromosome Location	chr5:144946914-144946915
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10036555	0.91[ASN][1000 genomes]
rs10053951	0.81[ASN][1000 genomes]
rs10062531	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10064198	0.91[ASN][1000 genomes]
rs10066886	0.91[ASN][1000 genomes]
rs10074155	0.92[ASN][1000 genomes]
rs10074645	0.91[ASN][1000 genomes]
rs10074797	0.91[ASN][1000 genomes]
rs10515551	0.92[ASN][1000 genomes]
rs11953390	0.91[ASN][1000 genomes]
rs13353880	0.91[ASN][1000 genomes]
rs13359453	0.91[ASN][1000 genomes]
rs13361864	0.91[ASN][1000 genomes]
rs1363555	0.92[ASN][1000 genomes]
rs1433029	0.91[ASN][1000 genomes]
rs1433031	0.91[ASN][1000 genomes]
rs1433033	0.91[ASN][1000 genomes]
rs1433034	0.91[ASN][1000 genomes]
rs1594673	0.91[ASN][1000 genomes]
rs17103424	0.91[ASN][1000 genomes]
rs17103425	0.91[ASN][1000 genomes]
rs1865005	0.92[ASN][1000 genomes]
rs1865009	0.91[ASN][1000 genomes]
rs1865010	0.91[ASN][1000 genomes]
rs1865011	0.90[ASN][1000 genomes]
rs1897582	0.81[ASN][1000 genomes]
rs1982071	0.91[ASN][1000 genomes]
rs2099326	0.91[ASN][1000 genomes]
rs2195937	0.91[ASN][1000 genomes]
rs2195938	0.81[ASN][1000 genomes]
rs28883046	0.91[ASN][1000 genomes]
rs35784567	0.92[ASN][1000 genomes]
rs4339405	0.81[ASN][1000 genomes]
rs4579305	0.81[ASN][1000 genomes]
rs4598024	0.88[ASN][1000 genomes]
rs56839506	0.91[ASN][1000 genomes]
rs57217872	0.98[ASN][1000 genomes]
rs57226270	0.92[ASN][1000 genomes]
rs60101315	0.91[ASN][1000 genomes]
rs62392708	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62394188	0.91[ASN][1000 genomes]
rs62394190	0.91[ASN][1000 genomes]
rs62394192	0.91[ASN][1000 genomes]
rs62394193	0.91[ASN][1000 genomes]
rs62394194	0.91[ASN][1000 genomes]
rs62394195	0.91[ASN][1000 genomes]
rs62394196	0.91[ASN][1000 genomes]
rs62394197	0.90[ASN][1000 genomes]
rs62394213	0.91[ASN][1000 genomes]
rs62394216	0.88[ASN][1000 genomes]
rs62394217	0.91[ASN][1000 genomes]
rs62394219	0.91[ASN][1000 genomes]
rs6580381	0.91[ASN][1000 genomes]
rs6859315	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6863005	0.81[ASN][1000 genomes]
rs6872440	0.82[ASN][1000 genomes]
rs6876768	0.81[ASN][1000 genomes]
rs6881485	0.81[ASN][1000 genomes]
rs6883831	0.81[ASN][1000 genomes]
rs6884591	0.91[ASN][1000 genomes]
rs6889689	0.91[ASN][1000 genomes]
rs73311527	0.88[ASN][1000 genomes]
rs73313747	0.81[ASN][1000 genomes]
rs73313748	0.81[ASN][1000 genomes]
rs7712910	0.91[ASN][1000 genomes]
rs953421	0.91[ASN][1000 genomes]
rs953422	0.91[ASN][1000 genomes]
rs964923	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9885537	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883004	chr5:144945649-145068001	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv883005	chr5:144945649-145107586	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	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	chr5:144924000-144949000	Weak transcription	Aorta	Aorta
2	chr5:144943200-144947600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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