Variant report

Variant	rs73935058
Chromosome Location	chr19:52745506-52745507
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	chr19:52745285..52748206-chr19:52749968..52752149,2	K562	blood:
2	chr19:52692216..52694566-chr19:52744371..52746217,2	K562	blood:

Variant related genes	Relation type
ENSG00000105568	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10407427	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10413108	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10416373	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10417447	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13343453	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16983619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16983638	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16983643	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16983648	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2059808	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28444225	0.85[AFR][1000 genomes]
rs28563055	0.85[AFR][1000 genomes]
rs4327163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55716802	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57370252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59065835	0.95[EUR][1000 genomes]
rs60307688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60998301	1.00[ASN][1000 genomes]
rs62110361	0.92[ASN][1000 genomes]
rs62110362	0.92[ASN][1000 genomes]
rs6509628	0.86[AFR][1000 genomes]
rs6509629	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7249557	0.92[ASN][1000 genomes]
rs7250109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7255737	0.86[AFR][1000 genomes]
rs7256125	0.86[AFR][1000 genomes]
rs7256300	0.87[AFR][1000 genomes]
rs7256312	0.87[AFR][1000 genomes]
rs7256719	0.86[AFR][1000 genomes]
rs73935075	1.00[EUR][1000 genomes]
rs73935076	1.00[EUR][1000 genomes]
rs73935077	1.00[EUR][1000 genomes]
rs73935078	1.00[EUR][1000 genomes]
rs73935079	1.00[EUR][1000 genomes]
rs8101776	1.00[ASN][1000 genomes]
rs8108037	0.92[ASN][1000 genomes]
rs8108693	0.92[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	nsv1065410	chr19:52103914-52889530	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	596 gene(s)	inside rSNPs	diseases
2	esv3366000	chr19:52491073-52842946	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv1066015	chr19:52502213-52890308	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv544059	chr19:52502213-52890308	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 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	chr19:52733200-52759600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr19:52734400-52751600	Weak transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links