Variant report

Variant	rs12474024
Chromosome Location	chr2:148461000-148461001
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1014064	0.81[TSI][hapmap]
rs10170800	0.82[EUR][1000 genomes]
rs10181608	0.82[EUR][1000 genomes]
rs10183294	0.82[EUR][1000 genomes]
rs10469566	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10497018	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497023	0.82[EUR][1000 genomes]
rs1113958	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1128919	0.81[TSI][hapmap]
rs12464481	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464921	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464985	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12465277	0.82[EUR][1000 genomes]
rs12467064	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12467429	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12468864	0.83[EUR][1000 genomes]
rs12691767	0.81[ASN][1000 genomes]
rs12988552	0.82[EUR][1000 genomes]
rs12998729	0.83[TSI][hapmap]
rs13004499	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13014274	0.82[EUR][1000 genomes]
rs13026223	0.83[EUR][1000 genomes]
rs13033070	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1364658	0.81[CEU][hapmap]
rs1406447	0.84[ASN][1000 genomes]
rs1424953	0.81[EUR][1000 genomes]
rs1528837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1528839	0.82[EUR][1000 genomes]
rs16827722	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1919440	0.82[EUR][1000 genomes]
rs1919441	0.82[EUR][1000 genomes]
rs35826590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35905220	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4662292	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4662293	0.83[EUR][1000 genomes]
rs4662548	0.84[ASN][1000 genomes]
rs6706259	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6721628	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6728992	0.82[EUR][1000 genomes]
rs7560139	0.82[EUR][1000 genomes]
rs7564409	0.82[EUR][1000 genomes]
rs7568718	0.83[EUR][1000 genomes]
rs7581116	0.81[ASN][1000 genomes]
rs7590862	0.82[EUR][1000 genomes]
rs7595433	0.81[ASN][1000 genomes]
rs7605932	0.83[EUR][1000 genomes]
rs929939	0.81[TSI][hapmap]
rs9653190	0.81[EUR][1000 genomes];0.83[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	nsv875275	chr2:148166428-148711242	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv916286	chr2:148438001-148977722	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12474024	ORC4L	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148459600-148462200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:148460200-148461800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr2:148460800-148461200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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