Variant report

Variant	rs36017423
Chromosome Location	chr1:84236639-84236640
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	chr1:84233925..84236856-chr1:84240562..84242799,2	K562	blood:
2	chr1:84233925..84236856-chr1:84240562..84242993,3	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10430047	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10430048	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10430063	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10430064	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10489501	0.82[AFR][1000 genomes]
rs10489502	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10489503	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10489504	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10874419	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10874420	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10874421	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10874422	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163826	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11163828	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11163829	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11163830	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11163832	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163833	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163835	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163837	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163838	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163839	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11163840	0.86[EUR][1000 genomes]
rs11163841	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11163842	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12035289	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12041369	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12044606	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12045391	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12059428	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12077325	0.80[AFR][1000 genomes]
rs12080974	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12085122	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12087099	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12088221	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12088867	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12091588	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12092736	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12093748	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17129275	0.86[ASN][1000 genomes]
rs17129297	0.86[ASN][1000 genomes]
rs17129321	0.86[ASN][1000 genomes]
rs17129344	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17129346	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17129416	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28476757	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4140461	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61766224	0.86[ASN][1000 genomes]
rs714280	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs717234	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72952444	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs74094961	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7529582	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs969125	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs969126	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs997869	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[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	esv33557	chr1:84236172-84236848	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv32823	chr1:84236604-84236848	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84236000-84237200	Enhancers	Liver	Liver
2	chr1:84236400-84237400	Weak transcription	Primary B cells from cord blood	blood

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