Variant report

Variant	rs67446783
Chromosome Location	chr6:142952243-142952244
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1070576	0.87[EUR][1000 genomes]
rs1070577	0.87[EUR][1000 genomes]
rs1098067	0.85[EUR][1000 genomes]
rs13217677	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1417359	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs263152	0.96[ASN][1000 genomes]
rs2664050	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs28514730	0.81[EUR][1000 genomes]
rs35670034	0.88[EUR][1000 genomes]
rs35781078	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56077882	0.91[EUR][1000 genomes]
rs6906209	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6916595	0.88[EUR][1000 genomes]
rs6917687	0.87[EUR][1000 genomes]
rs6921853	0.99[EUR][1000 genomes]
rs6939573	0.88[EUR][1000 genomes]
rs702294	0.87[EUR][1000 genomes]
rs702295	0.87[EUR][1000 genomes]
rs702296	0.87[EUR][1000 genomes]
rs702298	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7759020	0.88[EUR][1000 genomes]
rs844443	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9386003	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9390007	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs9390009	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9390011	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9403400	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9496420	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs9496423	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9496425	0.88[EUR][1000 genomes]
rs9496427	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9496428	0.88[EUR][1000 genomes]
rs9496429	0.88[EUR][1000 genomes]
rs9496432	0.91[EUR][1000 genomes]
rs9496434	0.91[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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr6:142946800-142956000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:142949000-142953000	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr6:142949400-142952600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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