Variant report

Variant	rs10821391
Chromosome Location	chr9:93161720-93161721
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:93160898..93163217-chr9:93166360..93169284,2	K562	blood:

Extended variants
information (count: 101 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10465158	0.83[EUR][1000 genomes]
rs10465163	0.83[EUR][1000 genomes]
rs10512198	0.82[EUR][1000 genomes]
rs10761349	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10761365	0.83[EUR][1000 genomes]
rs10761367	0.83[EUR][1000 genomes]
rs10761373	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs10821371	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10821396	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10821397	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10821399	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10821403	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10821416	0.83[EUR][1000 genomes]
rs10821417	0.83[EUR][1000 genomes]
rs10821418	0.83[EUR][1000 genomes]
rs10821419	0.82[EUR][1000 genomes]
rs10821420	0.83[EUR][1000 genomes]
rs10821421	0.83[EUR][1000 genomes]
rs10821422	0.83[EUR][1000 genomes]
rs10821423	0.83[EUR][1000 genomes]
rs10821424	0.83[EUR][1000 genomes]
rs10821425	0.83[EUR][1000 genomes]
rs10821426	0.83[EUR][1000 genomes]
rs10821427	0.83[EUR][1000 genomes]
rs10821429	0.83[EUR][1000 genomes]
rs10821434	0.83[EUR][1000 genomes]
rs10821435	0.83[EUR][1000 genomes]
rs10821443	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs10821444	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs10821445	0.83[EUR][1000 genomes]
rs10821448	0.81[EUR][1000 genomes]
rs10993252	0.84[EUR][1000 genomes]
rs10993310	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10993323	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10993468	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs10993469	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs10993470	0.83[EUR][1000 genomes]
rs12375952	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12377373	0.83[EUR][1000 genomes]
rs1343100	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1343101	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1529333	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs1571452	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1648476	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1754059	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1777013	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1777035	0.90[JPT][hapmap]
rs1889205	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2004205	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2114349	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2386534	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2555065	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2555066	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2555067	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2555068	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2771077	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2771080	0.90[JPT][hapmap]
rs2771081	0.90[JPT][hapmap]
rs2798049	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2798050	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2798053	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2892055	0.83[EUR][1000 genomes]
rs3748185	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs3748186	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs3748187	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs4237223	0.83[EUR][1000 genomes]
rs4237224	0.83[EUR][1000 genomes]
rs4405040	0.84[EUR][1000 genomes]
rs4595251	0.83[EUR][1000 genomes]
rs4743985	0.83[EUR][1000 genomes]
rs4743986	0.83[EUR][1000 genomes]
rs4743987	0.83[EUR][1000 genomes]
rs4744373	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4744385	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4744396	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4744413	0.82[EUR][1000 genomes]
rs4744414	0.82[EUR][1000 genomes]
rs4744415	0.83[EUR][1000 genomes]
rs4744416	0.83[EUR][1000 genomes]
rs4744417	0.83[EUR][1000 genomes]
rs4744418	0.83[EUR][1000 genomes]
rs4744439	0.83[EUR][1000 genomes]
rs6479595	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs7029610	0.87[CHB][hapmap];0.85[JPT][hapmap]
rs752788	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7862861	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7869492	0.81[EUR][1000 genomes]
rs7870764	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs883922	0.83[EUR][1000 genomes]
rs913619	0.83[EUR][1000 genomes]
rs913620	0.83[EUR][1000 genomes]
rs913621	0.83[EUR][1000 genomes]
rs913622	0.83[EUR][1000 genomes]
rs9332454	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs944901	0.83[EUR][1000 genomes]
rs944902	0.83[EUR][1000 genomes]
rs944903	0.83[EUR][1000 genomes]
rs944904	0.83[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	nsv1041278	chr9:92965701-93560454	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv482748	chr9:93123377-93279526	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv893565	chr9:93130796-93392332	Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10821391	RP11-389K14.3	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93158400-93162800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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