Variant report

Variant	rs10472063
Chromosome Location	chr5:57780869-57780870
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10037721	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10039062	0.88[EUR][1000 genomes]
rs10052714	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10055153	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10056153	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs10057028	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10063214	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10064698	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10064918	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10069804	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10069810	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10070522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1159072	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11748206	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11748233	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12186775	0.93[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13178332	0.92[CEU][hapmap]
rs1389308	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1508908	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1508909	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1508921	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1559240	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1565729	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1858087	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2011644	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2029690	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2408929	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4551014	0.96[YRI][hapmap];0.94[AFR][1000 genomes]
rs4700294	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4700295	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6450477	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6450479	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6872961	0.84[EUR][1000 genomes]
rs6879314	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs6886814	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6891070	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6892103	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6892457	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7704108	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7704785	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7708191	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7710737	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7721390	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7721538	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7722318	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7726376	0.87[EUR][1000 genomes]
rs9292162	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9292164	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9292167	0.88[EUR][1000 genomes]
rs963989	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs966269	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs966270	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598246	chr5:57777623-57785273	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57773200-57785400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:57778200-57782800	Enhancers	Primary B cells from peripheral blood	blood
3	chr5:57779000-57782400	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr5:57779400-57783600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:57780000-57781200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:57780400-57781000	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr5:57780400-57783000	Enhancers	Primary neutrophils fromperipheralblood	blood

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