Variant report

Variant	rs60442917
Chromosome Location	chr2:173390936-173390937
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11887938	0.83[AFR][1000 genomes]
rs11898822	0.80[AFR][1000 genomes]
rs12465442	0.84[ASN][1000 genomes]
rs12467358	0.85[ASN][1000 genomes]
rs12474168	0.85[ASN][1000 genomes]
rs12474995	0.85[ASN][1000 genomes]
rs12475916	0.84[ASN][1000 genomes]
rs12476126	0.83[ASN][1000 genomes]
rs12477247	0.85[ASN][1000 genomes]
rs12478465	0.85[ASN][1000 genomes]
rs12619242	0.85[ASN][1000 genomes]
rs12622687	0.85[ASN][1000 genomes]
rs13383151	0.85[ASN][1000 genomes]
rs13402061	0.85[ASN][1000 genomes]
rs1344272	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1574247	0.85[ASN][1000 genomes]
rs16860543	0.81[ASN][1000 genomes]
rs2178474	0.85[ASN][1000 genomes]
rs2293646	0.85[ASN][1000 genomes]
rs2293649	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2357415	0.85[ASN][1000 genomes]
rs3792260	0.85[ASN][1000 genomes]
rs4308101	0.85[ASN][1000 genomes]
rs4619573	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4972836	0.83[AFR][1000 genomes]
rs4972839	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4972841	0.80[ASN][1000 genomes]
rs56084828	0.82[ASN][1000 genomes]
rs57957394	0.85[ASN][1000 genomes]
rs58016698	0.85[ASN][1000 genomes]
rs58044442	0.85[ASN][1000 genomes]
rs59020762	0.85[ASN][1000 genomes]
rs59524026	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59610589	0.85[ASN][1000 genomes]
rs60275829	0.81[ASN][1000 genomes]
rs60446415	0.85[ASN][1000 genomes]
rs6755100	0.85[ASN][1000 genomes]
rs72892596	0.83[AFR][1000 genomes]
rs72894305	0.83[AFR][1000 genomes]
rs72894386	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7564591	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7564654	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7565216	0.85[ASN][1000 genomes]
rs7566921	0.83[AFR][1000 genomes]
rs7582972	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7591883	0.85[ASN][1000 genomes]
rs7609465	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173376400-173397400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:173387400-173395000	Weak transcription	Primary T cells from cord blood	blood
3	chr2:173390600-173391800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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