Variant report

Variant	rs7614322
Chromosome Location	chr3:67777268-67777269
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1037819	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1037820	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11717401	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11720476	0.84[EUR][1000 genomes]
rs11924244	0.86[AMR][1000 genomes]
rs11924309	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11925909	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12630936	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1459904	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1459905	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1459906	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1459908	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1459909	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17046864	0.84[EUR][1000 genomes]
rs2125811	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2362439	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4856797	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4856798	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4856881	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4856882	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4856885	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55833751	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6548740	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6548748	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6802973	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7617263	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7617448	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7627435	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7632493	0.94[EUR][1000 genomes]
rs7637890	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7649792	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9832460	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9843013	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9881852	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][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	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr3:67721400-67800400	Weak transcription	Left Ventricle	heart
2	chr3:67775000-67778400	Weak transcription	Liver	Liver
3	chr3:67775800-67777400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:67775800-67790200	Weak transcription	Psoas Muscle	Psoas

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