Variant report

Variant	rs73400158
Chromosome Location	chr12:87446023-87446024
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 174 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:147)

rs_ID	r²[population]
rs10858556	1.00[ASN][1000 genomes]
rs11104222	1.00[ASN][1000 genomes]
rs11104241	1.00[ASN][1000 genomes]
rs11104353	1.00[ASN][1000 genomes]
rs11608450	1.00[ASN][1000 genomes]
rs11608474	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11608923	0.92[ASN][1000 genomes]
rs11609545	1.00[ASN][1000 genomes]
rs11610202	1.00[ASN][1000 genomes]
rs11610240	1.00[ASN][1000 genomes]
rs11610610	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11612996	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11613608	1.00[ASN][1000 genomes]
rs11614902	1.00[ASN][1000 genomes]
rs11615328	1.00[ASN][1000 genomes]
rs12099694	1.00[ASN][1000 genomes]
rs12099773	1.00[ASN][1000 genomes]
rs12099774	1.00[ASN][1000 genomes]
rs12301215	1.00[ASN][1000 genomes]
rs12813003	0.92[ASN][1000 genomes]
rs17014297	1.00[AMR][1000 genomes]
rs17014343	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014345	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014347	0.84[ASN][1000 genomes]
rs17014350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17014352	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014355	1.00[ASN][1000 genomes]
rs17014357	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014359	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014361	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014363	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014366	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014369	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17014430	1.00[ASN][1000 genomes]
rs17040813	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28438801	1.00[ASN][1000 genomes]
rs34546765	0.92[ASN][1000 genomes]
rs35212803	0.92[ASN][1000 genomes]
rs35316438	0.92[ASN][1000 genomes]
rs35772317	1.00[ASN][1000 genomes]
rs55676823	1.00[ASN][1000 genomes]
rs55742281	1.00[ASN][1000 genomes]
rs55778807	1.00[ASN][1000 genomes]
rs56212508	1.00[ASN][1000 genomes]
rs58636507	0.91[ASN][1000 genomes]
rs59432611	1.00[ASN][1000 genomes]
rs59500185	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60530487	1.00[ASN][1000 genomes]
rs60718562	1.00[ASN][1000 genomes]
rs61619114	1.00[ASN][1000 genomes]
rs61951460	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs66473769	1.00[ASN][1000 genomes]
rs66489945	1.00[ASN][1000 genomes]
rs66507120	1.00[ASN][1000 genomes]
rs66520580	1.00[ASN][1000 genomes]
rs66543122	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66569903	1.00[ASN][1000 genomes]
rs66574092	1.00[ASN][1000 genomes]
rs66589206	1.00[ASN][1000 genomes]
rs66606466	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66624731	1.00[ASN][1000 genomes]
rs66629114	1.00[ASN][1000 genomes]
rs66680519	1.00[ASN][1000 genomes]
rs66721237	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66739429	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66761801	1.00[ASN][1000 genomes]
rs66796553	1.00[ASN][1000 genomes]
rs66824103	1.00[ASN][1000 genomes]
rs66881017	1.00[ASN][1000 genomes]
rs66920061	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66935924	1.00[ASN][1000 genomes]
rs66952248	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs66983270	1.00[ASN][1000 genomes]
rs66995551	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67126124	1.00[ASN][1000 genomes]
rs67136611	1.00[ASN][1000 genomes]
rs67152262	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67224165	1.00[ASN][1000 genomes]
rs67261476	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67311221	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67347619	1.00[ASN][1000 genomes]
rs67399263	1.00[ASN][1000 genomes]
rs67407309	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67434511	0.92[ASN][1000 genomes]
rs67448624	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67535999	1.00[ASN][1000 genomes]
rs67562061	1.00[ASN][1000 genomes]
rs67580367	1.00[ASN][1000 genomes]
rs67639118	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67642342	1.00[ASN][1000 genomes]
rs67654202	1.00[ASN][1000 genomes]
rs67687334	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67691941	1.00[ASN][1000 genomes]
rs67735893	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67748606	1.00[ASN][1000 genomes]
rs67751006	1.00[ASN][1000 genomes]
rs67755243	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67768352	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67823383	1.00[ASN][1000 genomes]
rs67825879	1.00[ASN][1000 genomes]
rs67840505	1.00[ASN][1000 genomes]
rs67980276	1.00[ASN][1000 genomes]
rs67982985	1.00[ASN][1000 genomes]
rs68008015	1.00[ASN][1000 genomes]
rs68009363	1.00[ASN][1000 genomes]
rs68030146	1.00[ASN][1000 genomes]
rs68133325	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs68145579	1.00[ASN][1000 genomes]
rs68166481	1.00[ASN][1000 genomes]
rs71078956	1.00[ASN][1000 genomes]
rs7305593	1.00[ASN][1000 genomes]
rs73175427	1.00[ASN][1000 genomes]
rs73175468	1.00[ASN][1000 genomes]
rs73175480	1.00[ASN][1000 genomes]
rs73175494	1.00[ASN][1000 genomes]
rs73179849	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73179855	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73179857	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73181416	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73181428	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73181432	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73181435	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73181441	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73192720	1.00[ASN][1000 genomes]
rs73192732	1.00[ASN][1000 genomes]
rs73192749	1.00[ASN][1000 genomes]
rs73192760	1.00[ASN][1000 genomes]
rs73393740	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73393778	1.00[AMR][1000 genomes]
rs73400125	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73408641	1.00[AMR][1000 genomes]
rs73408682	1.00[AMR][1000 genomes]
rs73410067	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73410102	1.00[AMR][1000 genomes]
rs73412009	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73412012	1.00[AMR][1000 genomes]
rs73412014	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73412072	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73412073	1.00[AMR][1000 genomes]
rs73412076	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73412087	1.00[AMR][1000 genomes]
rs73412095	1.00[AMR][1000 genomes]
rs73414089	1.00[AMR][1000 genomes]
rs73414095	1.00[AMR][1000 genomes]
rs73414099	1.00[AMR][1000 genomes]
rs73414185	1.00[AMR][1000 genomes]
rs73416003	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754127	chr12:86723232-87576932	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv916862	chr12:86837694-87718558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv899397	chr12:86863041-87636831	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv868879	chr12:87207243-87578373	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv559693	chr12:87216285-87447757	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1052693	chr12:87219949-87573582	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv899403	chr12:87225050-87528020	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2753551	chr12:87226774-87473947	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv899406	chr12:87233995-87528020	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv899407	chr12:87254691-87506910	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	esv2752961	chr12:87255339-87465826	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	esv2754599	chr12:87255339-87491053	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	esv2755612	chr12:87260646-87460465	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	esv2755080	chr12:87260646-87465826	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	esv2754967	chr12:87281456-87491053	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	nsv519543	chr12:87307329-87528020	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	nsv899408	chr12:87319908-87490752	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	nsv899409	chr12:87319908-87506910	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
19	nsv899410	chr12:87319908-87528020	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv899411	chr12:87339195-87459912	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
21	nsv899412	chr12:87346094-87506910	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv899413	chr12:87378980-87490752	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv899414	chr12:87378980-87506910	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv559698	chr12:87435308-87479405	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
25	nsv559699	chr12:87442480-87491505	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
26	nsv899415	chr12:87442480-87528020	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv899416	chr12:87442480-87588533	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87442000-87448400	Weak transcription	Fetal Brain Male	brain
2	chr12:87445200-87446200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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