Variant report

Variant	rs1097997
Chromosome Location	chr12:86555154-86555155
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10776954	0.83[CEU][hapmap]
rs10858411	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs10858412	0.83[CEU][hapmap]
rs11117162	1.00[ASW][hapmap];0.84[CEU][hapmap];0.86[GIH][hapmap]
rs11117189	1.00[CHB][hapmap]
rs1389292	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1389294	0.82[CEU][hapmap]
rs1389295	0.83[CEU][hapmap]
rs1463750	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1493414	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1493417	0.83[CEU][hapmap];0.81[TSI][hapmap]
rs1493418	0.83[CEU][hapmap]
rs1493419	0.92[TSI][hapmap]
rs1493420	0.82[TSI][hapmap]
rs1532263	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs1628799	0.89[CEU][hapmap];0.96[TSI][hapmap]
rs1689364	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs1698757	1.00[CHB][hapmap]
rs2405934	0.83[CEU][hapmap];0.81[TSI][hapmap]
rs2406128	0.83[CEU][hapmap]
rs2452803	0.83[CEU][hapmap];0.81[TSI][hapmap]
rs2452805	0.82[CEU][hapmap]
rs2452808	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs2471565	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs2471567	0.83[CEU][hapmap]
rs2897273	1.00[CHB][hapmap];0.84[TSI][hapmap];1.00[YRI][hapmap]
rs6538021	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6538023	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs6538027	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7134944	1.00[CHB][hapmap];0.92[GIH][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap]
rs7312245	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs7398950	0.81[GIH][hapmap]
rs7954833	1.00[CHB][hapmap];0.92[GIH][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap]
rs7961367	0.81[GIH][hapmap]
rs7965726	0.81[GIH][hapmap]
rs7967417	0.81[GIH][hapmap]
rs7972185	0.92[GIH][hapmap];0.80[TSI][hapmap]
rs839094	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839099	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs839100	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs839106	1.00[CHB][hapmap]
rs839107	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs839109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs839112	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839113	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839114	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs839115	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs839116	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs839117	1.00[CEU][hapmap]
rs839119	1.00[CHB][hapmap]
rs839120	1.00[CHB][hapmap]
rs839124	1.00[CHB][hapmap]
rs839128	1.00[CHB][hapmap]
rs839134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839138	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[MEX][hapmap];0.85[TSI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839139	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes]
rs839147	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs839162	0.83[CEU][hapmap];0.96[TSI][hapmap]
rs839183	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839185	1.00[ASN][1000 genomes]
rs839186	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs839187	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs839188	1.00[ASN][1000 genomes]
rs839189	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs839191	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs844433	0.89[CEU][hapmap]
rs844437	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs858213	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs866893	1.00[CHB][hapmap];1.00[ASN][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	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	esv2753278	chr12:86522507-86555154	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv510606	chr12:86545449-86555302	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

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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