Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10510658	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11129588	0.82[EUR][1000 genomes]
rs11129590	0.85[EUR][1000 genomes]
rs11708781	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11710773	0.85[EUR][1000 genomes]
rs11714874	0.82[EUR][1000 genomes]
rs11717932	1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11920101	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11927616	0.82[EUR][1000 genomes]
rs11927965	0.85[EUR][1000 genomes]
rs13063086	0.92[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs13065915	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13079510	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13083357	0.92[CEU][hapmap];1.00[GIH][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1866754	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2053425	1.00[JPT][hapmap]
rs66558495	0.81[EUR][1000 genomes]
rs6789334	0.85[GIH][hapmap]
rs7621412	1.00[CEU][hapmap]
rs7626572	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7627333	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs968102	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs968103	0.82[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	nsv522881	chr3:33736126-34241686	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1001599	chr3:34149575-34437701	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536533	chr3:34149575-34437701	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv876682	chr3:34149814-34401451	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv916961	chr3:34203879-34506554	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11129589	GADL1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34227800-34230600	Weak transcription	Thymus	Thymus
2	chr3:34228200-34228400	Enhancers	Small Intestine	intestine

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