Variant report

Variant	rs4575155
Chromosome Location	chr10:16217471-16217472
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10159534	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10737010	0.91[EUR][1000 genomes]
rs10737011	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10795356	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10904693	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1340133	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1340134	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1340137	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1340138	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1340139	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1417093	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1538762	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1577073	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1578266	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1591933	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1591934	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1832657	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1856726	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1890848	0.86[ASN][1000 genomes]
rs2151948	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2185386	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2486896	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2486906	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2883626	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2991895	0.90[EUR][1000 genomes]
rs4747265	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6602081	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6602082	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6602088	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7081816	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv894900	chr10:15285306-16232093	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv530146	chr10:15722937-16522747	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1049806	chr10:16065973-16228249	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3421318	chr10:16207333-16220262	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3337355	chr10:16207353-16220232	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16217400-16239000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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