Variant report

Variant	rs844433
Chromosome Location	chr12:86594024-86594025
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10506932	0.88[YRI][hapmap]
rs10776953	0.83[CEU][hapmap];0.83[YRI][hapmap];0.83[AMR][1000 genomes]
rs10776954	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs10776958	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10776960	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10776967	0.83[EUR][1000 genomes]
rs10858411	0.94[CEU][hapmap];0.83[EUR][1000 genomes]
rs10858412	0.83[CEU][hapmap]
rs10858417	0.82[EUR][1000 genomes]
rs10858420	0.89[CEU][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1097997	0.89[CEU][hapmap]
rs11103946	0.81[EUR][1000 genomes]
rs11829372	0.90[YRI][hapmap]
rs11830448	0.84[YRI][hapmap]
rs1389291	0.84[YRI][hapmap]
rs1389292	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1389294	0.83[CEU][hapmap]
rs1463750	1.00[CEU][hapmap]
rs1493408	0.84[CEU][hapmap]
rs1493414	0.94[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1493417	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs1493418	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs1493419	0.89[CEU][hapmap]
rs1493420	0.84[CEU][hapmap]
rs1532263	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1628799	1.00[CEU][hapmap]
rs1689364	1.00[CEU][hapmap]
rs17013792	0.86[YRI][hapmap]
rs17013833	0.83[YRI][hapmap]
rs17013842	0.89[YRI][hapmap]
rs17013858	0.84[YRI][hapmap]
rs1994863	0.91[EUR][1000 genomes]
rs2250915	0.80[CEU][hapmap]
rs2405934	0.83[CEU][hapmap]
rs2406120	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2406128	0.84[CEU][hapmap]
rs2452803	0.83[CEU][hapmap];0.80[EUR][1000 genomes]
rs2452805	0.83[CEU][hapmap]
rs2452808	0.94[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2465145	0.80[EUR][1000 genomes]
rs2465148	0.80[EUR][1000 genomes]
rs2471561	0.81[CEU][hapmap]
rs2471562	0.85[CEU][hapmap]
rs2471563	0.81[CEU][hapmap]
rs2471565	1.00[CEU][hapmap]
rs4329741	0.80[EUR][1000 genomes]
rs6538021	0.89[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538023	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6538027	0.94[CEU][hapmap]
rs7134944	0.88[CEU][hapmap]
rs7312245	0.94[CEU][hapmap]
rs7953494	0.80[EUR][1000 genomes]
rs7954833	0.88[CEU][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7966656	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7972185	0.88[CEU][hapmap]
rs839094	1.00[ASN][1000 genomes]
rs839099	0.90[CEU][hapmap]
rs839100	1.00[CEU][hapmap]
rs839106	0.85[CEU][hapmap]
rs839107	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839109	0.90[CEU][hapmap]
rs839112	0.89[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839113	1.00[ASN][1000 genomes]
rs839114	0.89[CEU][hapmap]
rs839116	0.89[CEU][hapmap]
rs839117	0.90[CEU][hapmap]
rs839134	0.90[CEU][hapmap];1.00[ASN][1000 genomes]
rs839138	0.89[CEU][hapmap];1.00[ASN][1000 genomes]
rs839139	0.90[CEU][hapmap]
rs839147	0.89[CEU][hapmap]
rs839162	0.94[CEU][hapmap]
rs839166	0.85[CEU][hapmap]
rs839183	0.89[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839185	1.00[ASN][1000 genomes]
rs839186	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839187	0.83[EUR][1000 genomes]
rs839188	1.00[ASN][1000 genomes]
rs839189	1.00[ASN][1000 genomes]
rs839191	1.00[ASN][1000 genomes]
rs844434	0.85[CEU][hapmap]
rs844437	0.90[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs858213	1.00[CEU][hapmap]
rs866893	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1053087	chr12:86569126-86733418	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv541564	chr12:86569126-86733418	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv800	chr12:86572379-86617887	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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