Variant report

Variant	rs36046073
Chromosome Location	chr3:22021211-22021212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E2-2	chr3:22021123-22021320	ENSG00000223351

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10510522	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11708529	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11708742	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11714027	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11714758	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11715520	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12485586	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12486230	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12490009	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12492135	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12494411	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13068226	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13074106	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13078946	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13088863	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1486392	0.87[ASN][1000 genomes]
rs1603667	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17010135	0.87[ASN][1000 genomes]
rs17010562	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1813534	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2336516	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34187078	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34256295	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34450884	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34866662	1.00[ASN][1000 genomes]
rs35063591	0.88[ASN][1000 genomes]
rs35225619	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35284987	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35631029	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35828697	0.87[ASN][1000 genomes]
rs61311503	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs71310296	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71310299	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71312018	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7636441	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7652319	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751992	chr3:21786893-22212357	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv948555	chr3:21786893-22212357	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1003085	chr3:21887971-22415107	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv834633	chr3:21918264-22088338	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv876616	chr3:21946847-22310622	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv876617	chr3:21955784-22310622	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1007663	chr3:21984364-22022923	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
8	nsv1001030	chr3:21985380-22022923	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv460474	chr3:21985417-22047934	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
10	nsv589932	chr3:21985417-22047934	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
11	nsv998319	chr3:21999480-22033364	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
12	nsv432404	chr3:22000296-22433396	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv876618	chr3:22005074-22057218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22020400-22022000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr3:22020800-22021800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:22021000-22021800	Enhancers	NH-A	brain

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