Variant report

Variant	rs13082318
Chromosome Location	chr3:25298421-25298422
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10510558	0.97[EUR][1000 genomes]
rs10510559	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10510560	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10510561	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13068143	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13068891	0.85[CEU][hapmap];1.00[YRI][hapmap]
rs13074533	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13085280	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13087573	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13087919	0.82[EUR][1000 genomes]
rs13088581	0.95[EUR][1000 genomes]
rs13090740	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13092896	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13093059	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13096074	0.94[EUR][1000 genomes]
rs1436239	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1436240	0.81[ASN][1000 genomes]
rs1561115	0.94[EUR][1000 genomes]
rs1601161	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1601162	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17015971	0.95[EUR][1000 genomes]
rs17015978	0.97[EUR][1000 genomes]
rs17016060	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17016078	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17016133	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17578259	0.82[EUR][1000 genomes]
rs1992059	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1992060	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34197182	0.85[EUR][1000 genomes]
rs34403304	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34537630	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34820979	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34985047	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35180299	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35264689	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35336027	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35508620	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35646412	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35888700	0.97[EUR][1000 genomes]
rs56062751	0.89[EUR][1000 genomes]
rs57402663	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61228958	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6550960	0.81[ASN][1000 genomes]
rs66807073	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs66939282	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67150539	0.97[EUR][1000 genomes]
rs67681308	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6779499	0.97[EUR][1000 genomes]
rs67880640	0.94[EUR][1000 genomes]
rs67912541	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6792184	0.97[EUR][1000 genomes]
rs68073275	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73042375	0.91[EUR][1000 genomes]
rs73042380	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73044294	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73045965	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7427426	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7430212	0.81[ASN][1000 genomes]
rs7432016	0.97[EUR][1000 genomes]
rs7632587	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949035	chr3:25194301-26084890	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
2	nsv508213	chr3:25206150-25326196	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1012646	chr3:25277328-25322125	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1006455	chr3:25277328-25327235	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25292200-25308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:25293000-25308400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:25298400-25299000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr3:25298400-25299400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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