Variant report

Variant	rs12315617
Chromosome Location	chr12:86700200-86700201
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 148 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10506931	0.84[CEU][hapmap]
rs10506934	1.00[CEU][hapmap]
rs10506935	0.87[CEU][hapmap];0.82[AMR][1000 genomes]
rs11830208	1.00[CEU][hapmap]
rs12304593	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12305255	0.93[CEU][hapmap];0.89[AMR][1000 genomes]
rs12306280	0.92[EUR][1000 genomes]
rs12306726	0.92[CEU][hapmap];0.89[AMR][1000 genomes]
rs12307279	1.00[CEU][hapmap]
rs12316480	1.00[CEU][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12582690	0.81[CEU][hapmap];0.94[EUR][1000 genomes]
rs1389296	0.86[CEU][hapmap]
rs1552840	0.85[CEU][hapmap]
rs17285589	0.92[CEU][hapmap]
rs17288772	0.93[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17288800	0.93[CEU][hapmap]
rs17289052	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17289087	1.00[CEU][hapmap]
rs17289115	1.00[CEU][hapmap]
rs17289150	1.00[CEU][hapmap]
rs17289178	1.00[CEU][hapmap]
rs17289646	1.00[CEU][hapmap]
rs17289938	0.87[CEU][hapmap]
rs17357233	0.86[CEU][hapmap]
rs17357259	0.83[CEU][hapmap]
rs17357469	0.85[CEU][hapmap]
rs17359446	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17367374	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17367869	1.00[CEU][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17367946	1.00[CEU][hapmap]
rs17369073	0.86[CEU][hapmap];0.82[AMR][1000 genomes]
rs1922743	0.93[CEU][hapmap];0.82[AMR][1000 genomes]
rs2405794	0.87[CEU][hapmap]
rs2405795	0.87[CEU][hapmap]
rs2406157	0.82[AMR][1000 genomes]
rs2406158	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs4842454	0.91[CEU][hapmap]
rs4842468	1.00[CEU][hapmap]
rs4842487	1.00[CEU][hapmap]
rs4842557	0.92[CEU][hapmap]
rs4842558	0.84[CEU][hapmap]
rs4842640	1.00[CEU][hapmap]
rs5022626	0.83[CEU][hapmap]
rs55649116	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55733909	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55820226	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55870715	0.82[AMR][1000 genomes]
rs55886852	0.81[AMR][1000 genomes]
rs55904324	0.82[AMR][1000 genomes]
rs55956857	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56293486	0.96[EUR][1000 genomes]
rs60436792	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61133374	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61948967	0.81[AMR][1000 genomes]
rs61948994	0.86[AMR][1000 genomes]
rs61949011	0.83[AMR][1000 genomes]
rs61949013	0.89[AMR][1000 genomes]
rs61949036	0.86[AMR][1000 genomes]
rs61949037	0.89[AMR][1000 genomes]
rs61949038	0.81[AMR][1000 genomes]
rs61949039	0.89[AMR][1000 genomes]
rs61949041	0.86[AMR][1000 genomes]
rs61949045	0.92[AMR][1000 genomes]
rs61949047	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61949048	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61949049	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61949475	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61949482	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61949483	0.92[EUR][1000 genomes]
rs61949532	0.82[AMR][1000 genomes]
rs61949533	0.82[AMR][1000 genomes]
rs61949558	0.82[AMR][1000 genomes]
rs61950663	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61950665	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61950667	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61950671	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61950674	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61950706	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950711	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950712	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950713	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61950714	0.98[EUR][1000 genomes]
rs61950746	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950747	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950748	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950749	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61950761	0.82[AMR][1000 genomes]
rs61950762	0.82[AMR][1000 genomes]
rs61950763	0.82[AMR][1000 genomes]
rs61950764	0.82[AMR][1000 genomes]
rs61950771	0.82[AMR][1000 genomes]
rs61950775	0.82[AMR][1000 genomes]
rs61950780	0.82[AMR][1000 genomes]
rs73189397	0.82[AMR][1000 genomes]
rs73191472	0.82[AMR][1000 genomes]
rs73191477	0.82[AMR][1000 genomes]
rs73191482	0.82[AMR][1000 genomes]
rs73191485	0.82[AMR][1000 genomes]
rs73191486	0.82[AMR][1000 genomes]
rs767898	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:48 , 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	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
6	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
7	nsv1037003	chr12:86610040-86798121	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	2 gene(s)	inside rSNPs	diseases
8	nsv1045386	chr12:86616015-86733418	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv541565	chr12:86616015-86733418	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv1843214	chr12:86673989-86703959	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv1850061	chr12:86673989-86703959	ZNF genes & repeats Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
12	nsv802	chr12:86683758-86723684	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv983491	chr12:86694812-86703018	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv2529439	chr12:86695010-86703868	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv2471686	chr12:86695246-86703977	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	nsv819565	chr12:86695439-86703271	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv2131445	chr12:86695532-86703230	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3490474	chr12:86695557-86703172	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3490452	chr12:86695594-86703143	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3490463	chr12:86695609-86703142	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3490496	chr12:86695621-86703419	Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3490485	chr12:86695628-86703098	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	nsv826467	chr12:86695659-86703171	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv514678	chr12:86695677-86703029	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	nsv498801	chr12:86695694-86703067	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3490508	chr12:86695695-86703067	Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv10267	chr12:86695700-86703035	Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv2421908	chr12:86695712-86701257	Weak transcription	n/a	n/a	inside rSNPs	diseases
29	nsv559684	chr12:86695712-86702395	Weak transcription	n/a	n/a	inside rSNPs	diseases
30	esv1843781	chr12:86695712-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv1851865	chr12:86695712-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
32	nsv559685	chr12:86695712-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
33	esv1845118	chr12:86695712-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv1845447	chr12:86695712-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
35	esv1847280	chr12:86695712-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
36	esv1850693	chr12:86695712-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
37	nsv826468	chr12:86695754-86703171	Weak transcription	n/a	n/a	inside rSNPs	diseases
38	esv1847809	chr12:86696771-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
39	esv1849878	chr12:86696771-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
40	esv1850450	chr12:86696771-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
41	esv1851205	chr12:86696771-86702906	Weak transcription	n/a	n/a	inside rSNPs	diseases
42	esv1844169	chr12:86696771-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
43	esv1846755	chr12:86696771-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
44	esv1846981	chr12:86696771-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
45	esv1849750	chr12:86696771-86703959	Weak transcription	n/a	n/a	inside rSNPs	diseases
46	esv1845250	chr12:86696771-86730126	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
47	nsv559686	chr12:86697440-86700407	Weak transcription	n/a	n/a	inside rSNPs	n/a
48	nsv559687	chr12:86697806-86702906	Weak transcription	n/a	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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