Variant report

Variant	rs768610
Chromosome Location	chr1:86771034-86771035
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10489735	0.99[ASN][1000 genomes]
rs10493789	0.80[CEU][hapmap];0.85[CHB][hapmap]
rs10747328	0.84[CHB][hapmap]
rs10873777	0.83[CEU][hapmap];0.84[CHB][hapmap]
rs1158505	0.85[CHB][hapmap]
rs11808143	0.98[ASN][1000 genomes]
rs1182102	0.83[CEU][hapmap]
rs12741520	1.00[ASN][1000 genomes]
rs12755828	0.99[ASN][1000 genomes]
rs1323027	1.00[ASN][1000 genomes]
rs1323029	1.00[ASN][1000 genomes]
rs1323030	1.00[ASN][1000 genomes]
rs1323031	1.00[ASN][1000 genomes]
rs1323033	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1323034	0.99[ASN][1000 genomes]
rs1334140	0.98[ASN][1000 genomes]
rs1334143	0.81[CHB][hapmap]
rs1334148	0.81[CHB][hapmap]
rs1575413	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1575414	1.00[ASN][1000 genomes]
rs1575415	0.99[ASN][1000 genomes]
rs17129055	0.87[ASN][1000 genomes]
rs175363	0.83[CEU][hapmap]
rs185655	0.81[CHB][hapmap]
rs1931363	0.84[CHB][hapmap]
rs2181419	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2208925	0.80[ASN][1000 genomes]
rs2390100	1.00[ASN][1000 genomes]
rs272491	0.85[CHB][hapmap]
rs272492	0.83[CEU][hapmap];0.80[CHB][hapmap]
rs272498	0.82[CEU][hapmap];0.82[CHB][hapmap]
rs272504	0.83[CEU][hapmap];0.84[CHB][hapmap]
rs272507	0.83[CEU][hapmap];0.84[CHB][hapmap]
rs272516	0.83[CEU][hapmap]
rs34747640	0.99[ASN][1000 genomes]
rs3765975	0.84[CHB][hapmap]
rs410807	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs450927	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs452865	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs567133	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs569912	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61800656	0.87[ASN][1000 genomes]
rs6660770	1.00[ASN][1000 genomes]
rs6673014	0.96[ASN][1000 genomes]
rs6685789	1.00[ASN][1000 genomes]
rs6689064	1.00[ASN][1000 genomes]
rs6692784	0.99[ASN][1000 genomes]
rs6695671	0.80[CEU][hapmap];0.85[CHB][hapmap]
rs6701074	1.00[ASN][1000 genomes]
rs6704104	1.00[ASN][1000 genomes]
rs7525626	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7527383	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7527390	0.99[ASN][1000 genomes]
rs7533682	0.99[ASN][1000 genomes]
rs7536173	1.00[ASN][1000 genomes]
rs7542133	0.99[ASN][1000 genomes]
rs7548881	0.99[ASN][1000 genomes]
rs9787365	0.87[ASN][1000 genomes]
rs990771	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs997641	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][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	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1003838	chr1:86591841-87212231	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1002541	chr1:86689088-86905902	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv871223	chr1:86724523-86784804	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv871866	chr1:86726619-86851420	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 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	chr1:86762800-86771400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:86770600-86789800	Weak transcription	Fetal Lung	lung

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