Variant report

Variant	rs71617425
Chromosome Location	chr5:61540968-61540969
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	chr5:61539494..61542163-chr5:61560247..61562435,2	K562	blood:
2	chr5:61539663..61541258-chr5:61560288..61563274,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1108158	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11742167	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11747516	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11750109	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12655562	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13155253	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13156695	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13161789	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162519	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162821	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13169321	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13170425	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13176923	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13178729	0.87[AMR][1000 genomes]
rs13181377	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13188046	0.87[ASN][1000 genomes]
rs13189446	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16890613	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16890618	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16890628	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16890634	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16890651	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16898838	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2059162	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2063255	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35311093	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35572300	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35672643	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35692500	0.93[ASN][1000 genomes]
rs35699711	0.87[AMR][1000 genomes]
rs35744020	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35746052	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35794032	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35808056	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35842742	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs36105063	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3776612	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3776614	0.87[AMR][1000 genomes]
rs3846465	0.81[ASN][1000 genomes]
rs4635894	0.81[ASN][1000 genomes]
rs71617421	0.93[ASN][1000 genomes]
rs71617426	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71617427	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71617428	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71631932	0.93[ASN][1000 genomes]
rs7446543	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs971965	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024090	chr5:61258759-61921150	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2757996	chr5:61403138-61687817	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv2759345	chr5:61403138-61748912	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats 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 target site	31 gene(s)	inside rSNPs	diseases
4	nsv830318	chr5:61415713-61623320	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1020255	chr5:61451792-62031365	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1027539	chr5:61457762-62000008	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	esv11317	chr5:61501951-61555756	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv821303	chr5:61501951-61555756	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1830053	chr5:61510046-61550324	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv10702	chr5:61510435-61552062	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv964860	chr5:61510512-61548253	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv1826874	chr5:61512183-61552823	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv1830196	chr5:61512352-61548378	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv2755585	chr5:61535831-61618595	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 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	chr5:61534400-61552000	Weak transcription	Fetal Muscle Leg	muscle

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