Variant report

Variant	rs7981855
Chromosome Location	chr13:93188373-93188374
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:93187246..93189629-chr13:93231804..93233615,2	K562	blood:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1180898	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1180900	0.89[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1180903	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1333675	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1333676	0.93[AFR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1333677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1360671	0.81[CHB][hapmap]
rs1413191	0.81[CHB][hapmap]
rs1629541	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17436336	0.81[CHB][hapmap]
rs1855367	0.81[CHB][hapmap]
rs2149059	0.88[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2149060	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap]
rs2149061	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2209832	0.89[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2374031	0.81[CHB][hapmap]
rs2769298	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2769299	0.89[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap]
rs2780742	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap]
rs2780743	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs364383	0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.93[YRI][hapmap]
rs373049	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4144426	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs4384477	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs449674	0.81[CHB][hapmap]
rs4542527	0.81[CHB][hapmap]
rs4773689	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6492610	0.81[CHB][hapmap]
rs6492611	0.87[CHB][hapmap]
rs722178	0.81[CHB][hapmap]
rs727986	0.81[CHB][hapmap]
rs7318268	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs7319531	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7329646	0.94[CHB][hapmap];0.96[YRI][hapmap]
rs7350692	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7983525	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7992204	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7993864	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7998089	0.81[CHB][hapmap]
rs9516087	0.93[CEU][hapmap];1.00[YRI][hapmap]
rs9516088	0.93[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.93[YRI][hapmap]
rs9516089	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs9516091	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs9523689	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9523690	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.81[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9523691	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9523692	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9523693	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9523701	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9556183	0.81[CHB][hapmap]
rs9556184	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9556188	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9561068	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap]
rs9561069	0.86[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs9561073	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9561074	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9561075	0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9561076	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9561077	0.93[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9561078	0.89[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9561079	0.81[CHB][hapmap]
rs9584032	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs974419	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.88[ASN][1000 genomes]
rs993485	0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471168	chr13:93138577-93208593	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
2	nsv900904	chr13:93138577-93208593	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900905	chr13:93138577-93211339	Enhancers Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv562728	chr13:93142706-93208593	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv456069	chr13:93161846-93204427	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv562729	chr13:93161846-93204427	Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	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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