Variant report

Variant	rs61372671
Chromosome Location	chr1:221719862-221719863
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:221716913..221720065-chr1:221720989..221725368,3	K562	blood:

Variant related genes	Relation type
ENSG00000227585	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10495165	0.94[ASN][1000 genomes]
rs10495166	0.94[ASN][1000 genomes]
rs10495167	0.94[ASN][1000 genomes]
rs10495168	0.94[ASN][1000 genomes]
rs12401875	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12403055	0.94[ASN][1000 genomes]
rs12404274	1.00[ASN][1000 genomes]
rs12405504	0.94[ASN][1000 genomes]
rs12409206	1.00[ASN][1000 genomes]
rs12410562	0.94[ASN][1000 genomes]
rs12411238	1.00[ASN][1000 genomes]
rs17010272	0.83[ASN][1000 genomes]
rs17010290	0.83[ASN][1000 genomes]
rs17010309	0.83[ASN][1000 genomes]
rs17041848	0.83[ASN][1000 genomes]
rs17041852	0.83[ASN][1000 genomes]
rs17041853	0.83[ASN][1000 genomes]
rs17661530	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35827283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58002157	0.94[ASN][1000 genomes]
rs58467896	0.94[ASN][1000 genomes]
rs58516053	0.94[ASN][1000 genomes]
rs58659812	0.94[ASN][1000 genomes]
rs58696164	0.94[ASN][1000 genomes]
rs60805607	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73106612	0.94[ASN][1000 genomes]
rs73106614	0.94[ASN][1000 genomes]
rs73106616	0.94[ASN][1000 genomes]
rs73106619	0.94[ASN][1000 genomes]
rs73106624	0.94[ASN][1000 genomes]
rs73106631	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73106634	0.83[ASN][1000 genomes]
rs73106648	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73116215	1.00[ASN][1000 genomes]
rs73116221	1.00[ASN][1000 genomes]
rs73117996	1.00[ASN][1000 genomes]
rs73117998	1.00[ASN][1000 genomes]
rs73118002	1.00[ASN][1000 genomes]
rs73119903	1.00[ASN][1000 genomes]
rs73119910	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73119916	0.94[ASN][1000 genomes]
rs73119926	0.94[ASN][1000 genomes]
rs73119928	0.94[ASN][1000 genomes]
rs73119929	0.94[ASN][1000 genomes]
rs73119932	0.94[ASN][1000 genomes]
rs73119935	0.94[ASN][1000 genomes]
rs73119938	0.94[ASN][1000 genomes]
rs73119939	0.94[ASN][1000 genomes]
rs73119945	0.94[ASN][1000 genomes]
rs73119947	0.94[ASN][1000 genomes]
rs73119948	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873200	chr1:221644180-221843191	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1009838	chr1:221692621-221773945	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv535301	chr1:221692621-221773945	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221717600-221721400	Weak transcription	Liver	Liver

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