Variant report

Variant	rs9561079
Chromosome Location	chr13:93154482-93154483
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:93142214..93145104-chr13:93152778..93154703,2	K562	blood:

Variant related genes	Relation type
ENSG00000263741	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1180898	0.86[CHB][hapmap]
rs1180900	0.87[CHB][hapmap]
rs12874576	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1333675	0.81[CHB][hapmap]
rs1333677	0.81[CHB][hapmap]
rs1360671	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1413191	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs1629541	0.81[CHB][hapmap]
rs16947810	0.83[ASN][1000 genomes]
rs17436336	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1855367	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap]
rs2149059	0.87[CHB][hapmap]
rs2149060	0.81[CHB][hapmap]
rs2149061	0.81[CHB][hapmap]
rs2209829	0.90[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2209832	0.81[CHB][hapmap]
rs2374031	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2769299	0.81[YRI][hapmap]
rs2780742	0.81[CHB][hapmap]
rs2780744	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs364383	0.81[CHB][hapmap]
rs4144426	0.81[CHB][hapmap]
rs4384477	0.81[CHB][hapmap]
rs449674	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4542527	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs55803730	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6492610	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6492611	0.95[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6492616	0.87[ASN][1000 genomes]
rs722178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs727986	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7317407	0.85[EUR][1000 genomes]
rs7318268	0.85[CHB][hapmap]
rs7490474	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7981855	0.81[CHB][hapmap]
rs7984374	0.82[ASN][1000 genomes]
rs7984842	0.82[ASN][1000 genomes]
rs7992204	0.81[CHB][hapmap]
rs7993864	0.81[CHB][hapmap]
rs7998089	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9516088	0.81[CHB][hapmap]
rs9516089	0.87[CHB][hapmap]
rs9516091	0.81[CHB][hapmap]
rs9523689	0.81[CHB][hapmap]
rs9523690	0.81[CHB][hapmap]
rs9523692	0.81[CHB][hapmap]
rs9523693	0.81[CHB][hapmap]
rs9556183	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9556188	0.81[CHB][hapmap]
rs9561068	0.81[CHB][hapmap]
rs9561069	0.81[CHB][hapmap]
rs9561073	0.81[CHB][hapmap]
rs9561075	0.81[CHB][hapmap]
rs9561076	0.81[CHB][hapmap]
rs9561077	0.81[CHB][hapmap]
rs9561078	0.81[CHB][hapmap];0.83[YRI][hapmap]
rs9561080	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9584032	0.81[CHB][hapmap]
rs974419	0.81[CHB][hapmap]
rs993485	0.81[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	nsv562728	chr13:93142706-93208593	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93153000-93160200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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