Variant report

Variant	rs4680468
Chromosome Location	chr3:151197138-151197139
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:151194512..151197390-chr3:151199277..151201017,2	K562	blood:
2	chr3:151194378..151197390-chr3:151198956..151201017,3	K562	blood:
3	chr3:151189546..151191159-chr3:151195430..151197288,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11712630	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12630095	0.85[EUR][1000 genomes]
rs12634284	0.82[ASN][1000 genomes]
rs12639049	0.82[ASN][1000 genomes]
rs13315624	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4128734	0.84[ASN][1000 genomes]
rs4234330	0.82[EUR][1000 genomes]
rs4296566	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4350898	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4455304	0.84[EUR][1000 genomes]
rs4481136	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4484172	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4608665	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4679836	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4679837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4680464	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4680465	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4680473	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6440744	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6440745	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6440748	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6789915	0.82[EUR][1000 genomes]
rs6798066	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7375135	0.82[ASN][1000 genomes]
rs7427979	0.84[EUR][1000 genomes]
rs7629172	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7631395	0.84[EUR][1000 genomes]
rs7636304	0.87[ASN][1000 genomes]
rs7637619	0.80[ASN][1000 genomes]
rs7647576	0.85[ASN][1000 genomes]
rs9289839	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9289840	0.89[AFR][1000 genomes]
rs9289847	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9680970	0.85[ASN][1000 genomes]
rs9808949	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9811565	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9817125	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9822315	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9837972	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9846323	0.82[ASN][1000 genomes]
rs9849929	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9856077	0.81[EUR][1000 genomes]
rs9863245	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9869975	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829757	chr3:151044880-151226442	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1000355	chr3:151108859-151243835	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv877649	chr3:151147968-151236562	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv877650	chr3:151174010-151314449	Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv963536	chr3:151191085-151212472	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv819466	chr3:151196634-151219966	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151193800-151197600	Enhancers	Fetal Lung	lung
2	chr3:151195600-151198400	Enhancers	Fetal Stomach	stomach
3	chr3:151196400-151209000	Weak transcription	Ovary	ovary
4	chr3:151196600-151197600	Weak transcription	Colon Smooth Muscle	Colon

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