Variant report

Variant	rs10050657
Chromosome Location	chr5:151241733-151241734
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10062169	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10065313	0.82[ASN][1000 genomes]
rs10078632	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10079787	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10463320	0.93[ASN][1000 genomes]
rs10476776	0.83[ASN][1000 genomes]
rs10476778	0.80[ASN][1000 genomes]
rs11167557	0.87[ASN][1000 genomes]
rs11167559	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12108921	0.94[ASN][1000 genomes]
rs12109022	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12109585	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12658422	0.83[ASN][1000 genomes]
rs1366238	0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1428159	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1428160	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2033212	0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2913878	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2913879	0.92[ASN][1000 genomes]
rs2913881	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2913882	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2913888	0.94[ASN][1000 genomes]
rs2913889	0.94[ASN][1000 genomes]
rs2913892	0.94[ASN][1000 genomes]
rs2913893	0.94[ASN][1000 genomes]
rs2913894	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2915885	0.83[ASN][1000 genomes]
rs2964596	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2964597	0.92[ASN][1000 genomes]
rs2964599	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2964601	0.94[ASN][1000 genomes]
rs2964603	0.94[ASN][1000 genomes]
rs2964604	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2964606	0.94[ASN][1000 genomes]
rs35692301	0.85[ASN][1000 genomes]
rs4075273	0.94[ASN][1000 genomes]
rs4076138	0.94[ASN][1000 genomes]
rs4259159	0.94[ASN][1000 genomes]
rs4331885	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4360031	0.83[ASN][1000 genomes]
rs4362933	0.83[ASN][1000 genomes]
rs4379180	0.83[ASN][1000 genomes]
rs4478307	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4541649	0.80[ASN][1000 genomes]
rs4555782	0.83[ASN][1000 genomes]
rs4594844	0.83[ASN][1000 genomes]
rs4629583	0.82[ASN][1000 genomes]
rs62394144	0.85[ASN][1000 genomes]
rs6579906	0.80[ASN][1000 genomes]
rs6579908	0.83[ASN][1000 genomes]
rs6579909	0.83[ASN][1000 genomes]
rs6579910	0.80[ASN][1000 genomes]
rs6863833	0.88[ASN][1000 genomes]
rs6863837	0.88[ASN][1000 genomes]
rs6868371	0.94[ASN][1000 genomes]
rs6870491	0.93[ASN][1000 genomes]
rs6878691	0.94[ASN][1000 genomes]
rs6892117	0.89[ASN][1000 genomes]
rs6896518	0.94[ASN][1000 genomes]
rs6896664	0.89[ASN][1000 genomes]
rs72802219	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7341167	0.88[ASN][1000 genomes]
rs7702751	0.87[ASN][1000 genomes]
rs7711609	0.94[ASN][1000 genomes]
rs7711771	0.94[ASN][1000 genomes]
rs7712779	0.93[ASN][1000 genomes]
rs7725327	0.94[ASN][1000 genomes]
rs7728956	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7729026	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7733241	0.83[ASN][1000 genomes]
rs9324712	0.94[ASN][1000 genomes]
rs9324714	0.85[AMR][1000 genomes];0.89[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	esv1808837	chr5:151238149-151260215	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 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	chr5:151231200-151242800	Weak transcription	Aorta	Aorta
2	chr5:151235200-151264200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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