Variant report

Variant	rs11901541
Chromosome Location	chr2:53188983-53188984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10490579	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17039478	1.00[ASN][1000 genomes]
rs17043734	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043739	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043781	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17043797	1.00[ASN][1000 genomes]
rs17043801	1.00[ASN][1000 genomes]
rs17043805	1.00[ASN][1000 genomes]
rs17043807	1.00[ASN][1000 genomes]
rs17043809	1.00[ASN][1000 genomes]
rs17571144	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116006	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34049687	0.80[EUR][1000 genomes]
rs56286124	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62128205	0.80[EUR][1000 genomes]
rs62138243	1.00[ASN][1000 genomes]
rs62138246	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62138247	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62138248	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62138249	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62138250	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140275	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140277	0.85[EUR][1000 genomes]
rs62140278	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140279	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140280	1.00[ASN][1000 genomes]
rs62140281	1.00[ASN][1000 genomes]
rs62140283	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140284	0.85[EUR][1000 genomes]
rs62140285	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140286	1.00[ASN][1000 genomes]
rs62140287	0.88[EUR][1000 genomes]
rs62140291	1.00[ASN][1000 genomes]
rs62140292	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72793423	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72793432	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998380	chr2:52891706-53222155	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1010978	chr2:52959769-53249951	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv520722	chr2:53039770-53421015	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv581978	chr2:53091691-53227749	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	nsv874136	chr2:53101066-53218774	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
6	nsv874137	chr2:53114775-53216917	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
7	nsv874138	chr2:53114775-53218774	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
8	esv3693331	chr2:53159702-53192269	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv963875	chr2:53173006-53196302	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
10	nsv1012463	chr2:53187151-53377118	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53185800-53194000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:53188600-53193200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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