Variant report

Variant	rs17144539
Chromosome Location	chr5:118087518-118087519
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1156413	1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1397582	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1397583	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1473231	1.00[AMR][1000 genomes]
rs1510975	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17144532	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17144540	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17144549	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17144571	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17144580	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17144586	0.95[ASN][1000 genomes]
rs17144591	0.95[ASN][1000 genomes]
rs17144596	0.95[ASN][1000 genomes]
rs17144602	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17144603	1.00[ASN][1000 genomes]
rs17144604	1.00[ASN][1000 genomes]
rs17144620	0.85[ASN][1000 genomes]
rs17144623	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17144624	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17144636	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17144640	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17144648	1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17144657	1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17144664	0.90[AMR][1000 genomes]
rs17144732	1.00[AMR][1000 genomes]
rs17144738	1.00[AMR][1000 genomes]
rs17144744	1.00[AMR][1000 genomes]
rs17144795	1.00[AMR][1000 genomes]
rs17144813	1.00[AMR][1000 genomes]
rs17144818	1.00[AMR][1000 genomes]
rs6880225	0.90[AMR][1000 genomes]
rs918389	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032241	chr5:117900051-118157400	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv882767	chr5:117931730-118385691	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 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	chr5:118085400-118088200	Weak transcription	Fetal Lung	lung

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