Variant report

Variant	rs12429205
Chromosome Location	chr13:89192725-89192726
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1124177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs12584429	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12875484	0.98[ASN][1000 genomes]
rs12877576	0.89[ASN][1000 genomes]
rs1334171	0.98[ASN][1000 genomes]
rs1334176	0.89[ASN][1000 genomes]
rs1334177	0.85[ASN][1000 genomes]
rs1334187	0.92[ASN][1000 genomes]
rs1455405	0.98[ASN][1000 genomes]
rs1577146	0.89[ASN][1000 genomes]
rs2124259	0.98[ASN][1000 genomes]
rs2347147	0.92[ASN][1000 genomes]
rs2881561	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs3963390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs4272895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4516077	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4531598	0.90[ASN][1000 genomes]
rs4772983	0.98[ASN][1000 genomes]
rs56250140	0.80[ASN][1000 genomes]
rs7319397	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7325451	0.97[ASN][1000 genomes]
rs7491890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7491918	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9514926	0.88[ASN][1000 genomes]
rs9514939	0.98[ASN][1000 genomes]
rs9514979	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9521076	0.98[ASN][1000 genomes]
rs9521104	0.90[ASN][1000 genomes]
rs9521105	0.98[ASN][1000 genomes]
rs9521106	0.98[ASN][1000 genomes]
rs9521107	0.95[ASN][1000 genomes]
rs9521140	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9521352	0.92[ASN][1000 genomes]
rs9521387	0.89[ASN][1000 genomes]
rs9521394	0.89[ASN][1000 genomes]
rs9559491	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9559492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9587704	0.88[ASN][1000 genomes]
rs9587710	0.93[ASN][1000 genomes]
rs9587714	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900815	chr13:89098616-89216190	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv870345	chr13:89164439-89295782	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3443995	chr13:89192251-89196549	Inactive region	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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