Variant report

Variant	rs13103819
Chromosome Location	chr4:73704442-73704443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10004087	0.89[ASN][1000 genomes]
rs10021333	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10155153	0.92[ASN][1000 genomes]
rs12647893	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13129078	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13129666	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13143720	0.89[ASN][1000 genomes]
rs1582753	0.91[ASN][1000 genomes]
rs1599448	0.93[ASN][1000 genomes]
rs167561	0.92[ASN][1000 genomes]
rs16848812	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs190095	0.85[ASN][1000 genomes]
rs192876	0.91[ASN][1000 genomes]
rs2126207	0.92[ASN][1000 genomes]
rs221594	0.91[ASN][1000 genomes]
rs2219625	0.91[ASN][1000 genomes]
rs2614299	0.92[ASN][1000 genomes]
rs315316	0.92[ASN][1000 genomes]
rs315326	0.86[ASN][1000 genomes]
rs315329	0.88[ASN][1000 genomes]
rs315333	0.91[ASN][1000 genomes]
rs315334	0.91[ASN][1000 genomes]
rs315341	0.92[ASN][1000 genomes]
rs315363	0.91[ASN][1000 genomes]
rs315368	0.91[ASN][1000 genomes]
rs315374	0.89[ASN][1000 genomes]
rs35038748	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35784055	0.86[ASN][1000 genomes]
rs4694143	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4694144	0.93[ASN][1000 genomes]
rs4694548	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4694549	0.86[ASN][1000 genomes]
rs4694557	0.93[ASN][1000 genomes]
rs4694574	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4694576	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4694577	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56334611	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs922254	0.86[ASN][1000 genomes]
rs922255	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949371	chr4:73678470-74094500	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv2757068	chr4:73683018-73770378	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2759261	chr4:73683018-73770378	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv436952	chr4:73693532-73759117	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv437923	chr4:73699066-73758650	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:73687200-73707800	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links