Variant report

Variant	rs1817735
Chromosome Location	chr6:74980974-74980975
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11752920	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11754468	0.86[EUR][1000 genomes]
rs11758445	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11759133	0.86[EUR][1000 genomes]
rs16884519	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16884624	1.00[EUR][1000 genomes]
rs16884690	0.98[EUR][1000 genomes]
rs3898077	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55768795	0.81[EUR][1000 genomes]
rs55784940	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55962148	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56004196	0.85[AMR][1000 genomes]
rs56020332	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56168817	0.98[EUR][1000 genomes]
rs56232317	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs67076726	1.00[EUR][1000 genomes]
rs6926572	0.98[EUR][1000 genomes]
rs72950543	1.00[AMR][1000 genomes]
rs72950546	1.00[AMR][1000 genomes]
rs72953763	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72954314	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72957983	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72957986	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72957999	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72959615	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72959617	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72959619	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72964214	0.85[AMR][1000 genomes]
rs72967265	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72967284	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72967286	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72967291	0.86[EUR][1000 genomes]
rs7755776	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776273	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9359077	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886162	chr6:74903797-75006170	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv886163	chr6:74944460-75006170	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv886164	chr6:74944460-75024313	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2758061	chr6:74961996-75128165	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2759442	chr6:74961996-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2829863	chr6:74976178-75040446	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv7920	chr6:74979517-74986088	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74979400-74987400	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:74979600-74983800	Weak transcription	Fetal Stomach	stomach

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