Variant report

Variant	rs35149900
Chromosome Location	chr4:101829280-101829281
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10001585	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10010483	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10010839	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10012835	0.97[ASN][1000 genomes]
rs10013351	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10019942	0.86[EUR][1000 genomes]
rs10049744	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1032571	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12646623	0.99[EUR][1000 genomes]
rs12710943	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13101247	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13102756	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13117493	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13118293	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13121097	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13124911	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13132631	0.98[EUR][1000 genomes]
rs13133911	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13137995	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13140872	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13142917	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13148044	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13434725	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13434734	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13435486	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1587240	0.98[EUR][1000 genomes]
rs17030617	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17030633	0.86[EUR][1000 genomes]
rs2132697	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2220988	0.98[EUR][1000 genomes]
rs2866249	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2866250	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28707515	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28791596	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28814048	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28849460	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28897071	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34205475	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34381813	0.99[EUR][1000 genomes]
rs34384213	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34389434	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34524820	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34571175	0.98[EUR][1000 genomes]
rs34921100	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34971704	0.81[EUR][1000 genomes]
rs35360493	0.82[EUR][1000 genomes]
rs35614617	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35632784	0.82[EUR][1000 genomes]
rs35938895	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36038282	0.82[EUR][1000 genomes]
rs36112244	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4698838	0.81[EUR][1000 genomes]
rs4699162	0.98[EUR][1000 genomes]
rs4699218	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62307728	0.98[EUR][1000 genomes]
rs6532915	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67935705	0.99[EUR][1000 genomes]
rs6817249	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6817484	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6840166	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6846371	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71614671	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7694484	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7694622	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7695271	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7695375	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7696336	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[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	nsv931418	chr4:101500167-102443207	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:101828800-101829400	Enhancers	Adipose Nuclei	Adipose
2	chr4:101828800-101829400	Enhancers	Fetal Intestine Small	intestine
3	chr4:101828800-101829600	Enhancers	HepG2	liver
4	chr4:101829000-101829400	Enhancers	Fetal Intestine Large	intestine
5	chr4:101829200-101829400	Flanking Active TSS	Liver	Liver
6	chr4:101829200-101837400	Weak transcription	Pancreas	Pancrea

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