Variant report

Variant	rs7434131
Chromosome Location	chr3:24046429-24046430
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11915299	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1533141	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1567579	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1567580	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1986889	0.80[EUR][1000 genomes]
rs34812592	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35755171	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35755253	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4858099	0.82[AMR][1000 genomes]
rs4858571	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6550830	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6550831	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6806085	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71324126	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7372315	0.81[AMR][1000 genomes]
rs7426647	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs954748	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv834638	chr3:23963860-24117191	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv834639	chr3:24037113-24233925	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv536523	chr3:24041166-24076110	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24036000-24053400	Weak transcription	Psoas Muscle	Psoas
2	chr3:24045600-24047600	Enhancers	NHEK	skin
3	chr3:24046400-24051800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:24046400-24060200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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