Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10741030	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828470	0.81[EUR][1000 genomes]
rs10828475	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11013474	0.80[CHB][hapmap]
rs11013481	0.80[CHB][hapmap]
rs11013484	0.80[CHB][hapmap]
rs11013543	0.81[EUR][1000 genomes]
rs11013549	0.81[EUR][1000 genomes]
rs11013557	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12244668	0.80[EUR][1000 genomes]
rs12571351	0.80[CHB][hapmap]
rs1337324	0.80[EUR][1000 genomes]
rs1337325	0.81[EUR][1000 genomes]
rs1415418	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16923259	0.80[CHB][hapmap]
rs1856113	0.81[EUR][1000 genomes]
rs1984173	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1985697	0.81[EUR][1000 genomes]
rs4008949	0.81[EUR][1000 genomes]
rs4387257	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4570482	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4748891	0.80[CHB][hapmap]
rs6482291	0.80[EUR][1000 genomes]
rs6482292	0.80[EUR][1000 genomes]
rs7079866	0.80[CHB][hapmap]
rs7097155	0.81[EUR][1000 genomes]
rs7907290	0.86[EUR][1000 genomes]
rs7913401	0.80[EUR][1000 genomes]
rs9633627	0.80[CHB][hapmap]
rs9633648	0.80[CHB][hapmap]
rs983989	0.81[EUR][1000 genomes]
rs983990	0.81[EUR][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	nsv831811	chr10:23734326-23913370	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv466835	chr10:23801555-23869175	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv550215	chr10:23801555-23869175	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23820400-23823200	Weak transcription	Primary T cells from cord blood	blood
2	chr10:23820800-23823200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:23820800-23823200	Weak transcription	Dnd41	blood
4	chr10:23821600-23824600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr10:23821600-23824600	Weak transcription	Monocytes-CD14+_RO01746	blood

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