Variant report

Variant	rs17673134
Chromosome Location	chr1:195731020-195731021
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:195720981..195722711-chr1:195730556..195732740,2	K562	blood:
2	chr1:195728301..195731398-chr1:195733712..195736941,3	MCF-7	breast:
3	chr1:195728899..195731213-chr1:195731741..195733671,2	K562	blood:
4	chr1:195729478..195731927-chr1:195733670..195735429,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10801449	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10921892	0.88[EUR][1000 genomes]
rs10921902	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11587693	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11587700	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11802328	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12074167	0.88[EUR][1000 genomes]
rs12083340	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12083881	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1576764	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17626633	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17626902	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17672688	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2895785	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2942913	0.95[ASN][1000 genomes]
rs2989981	0.95[ASN][1000 genomes]
rs4304556	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4335360	0.91[ASN][1000 genomes]
rs4514223	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55707019	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55894754	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56012771	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56024053	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56067913	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734142	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734144	0.88[EUR][1000 genomes]
rs72734150	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72734151	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72734153	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72734155	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72734156	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72734157	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72734159	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72734164	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734165	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734166	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734169	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72734170	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72736158	0.91[ASN][1000 genomes]
rs7415128	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872894	chr1:195053221-195745968	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv872932	chr1:195447286-195736070	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv872937	chr1:195493538-195849028	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1007203	chr1:195672857-195902360	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region 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	chr1:195730600-195732800	Weak transcription	Hela-S3	cervix

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