Variant report

Variant	rs11205072
Chromosome Location	chr1:152653531-152653532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs1011297	0.85[ASN][1000 genomes]
rs10788844	0.87[ASN][1000 genomes]
rs10888504	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs10888505	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs10888506	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10888507	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10888509	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs11205045	0.85[ASN][1000 genomes]
rs11205046	0.85[ASN][1000 genomes]
rs11205047	0.85[ASN][1000 genomes]
rs11205048	0.85[ASN][1000 genomes]
rs11205049	0.85[ASN][1000 genomes]
rs11205050	0.85[ASN][1000 genomes]
rs11205056	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11205060	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs11205061	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11205062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11205066	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11205073	0.85[CHB][hapmap];0.87[ASN][1000 genomes]
rs11205078	0.85[CHB][hapmap];0.86[ASN][1000 genomes]
rs11205080	1.00[CEU][hapmap]
rs11205084	1.00[CEU][hapmap]
rs11580546	0.85[ASN][1000 genomes]
rs11581621	0.85[ASN][1000 genomes]
rs11582021	0.85[ASN][1000 genomes]
rs11587218	0.85[ASN][1000 genomes]
rs12032251	0.85[ASN][1000 genomes]
rs12041270	0.85[ASN][1000 genomes]
rs12043198	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12071335	0.83[ASN][1000 genomes]
rs12074783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12081753	0.85[ASN][1000 genomes]
rs12081793	0.85[ASN][1000 genomes]
rs12239432	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12239456	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12564254	0.85[ASN][1000 genomes]
rs12564476	0.83[ASN][1000 genomes]
rs12566080	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12728742	0.85[ASN][1000 genomes]
rs12745646	0.85[ASN][1000 genomes]
rs12752346	0.85[ASN][1000 genomes]
rs1325508	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1332497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1359515	0.85[ASN][1000 genomes]
rs1359516	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1412542	0.86[CHB][hapmap]
rs1474168	0.85[ASN][1000 genomes]
rs1474169	0.85[ASN][1000 genomes]
rs1575753	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1581802	0.85[ASN][1000 genomes]
rs1581804	0.85[ASN][1000 genomes]
rs16834343	0.82[EUR][1000 genomes]
rs1819470	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1853805	0.87[ASN][1000 genomes]
rs1886732	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1888966	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925661	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1925663	0.86[ASN][1000 genomes]
rs1930126	0.86[CHB][hapmap];0.87[ASN][1000 genomes]
rs2224986	1.00[CEU][hapmap]
rs3753453	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3904413	0.86[CHB][hapmap]
rs3904414	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3904415	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3908717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4287181	0.86[ASN][1000 genomes]
rs4320779	0.85[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4353096	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4540662	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4845317	0.85[CHB][hapmap];0.86[ASN][1000 genomes]
rs4845456	0.83[CHB][hapmap];0.85[ASN][1000 genomes]
rs4845457	0.85[ASN][1000 genomes]
rs55644922	0.85[ASN][1000 genomes]
rs55687384	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59349974	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59540569	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59633986	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59863780	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60208884	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60350222	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60861680	0.85[ASN][1000 genomes]
rs66587527	0.89[ASN][1000 genomes]
rs6660162	0.85[ASN][1000 genomes]
rs6662989	0.85[ASN][1000 genomes]
rs6671975	0.85[ASN][1000 genomes]
rs6687570	0.85[ASN][1000 genomes]
rs6687682	0.85[ASN][1000 genomes]
rs6702474	0.85[ASN][1000 genomes]
rs73009167	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7527788	0.85[ASN][1000 genomes]
rs908929	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs925976	0.85[ASN][1000 genomes]
rs925977	0.85[ASN][1000 genomes]
rs942826	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs942827	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs960752	0.85[ASN][1000 genomes]
rs989831	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs989832	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs989833	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs989834	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9970033	0.85[ASN][1000 genomes]
rs9970657	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2750810	chr1:152453669-152660927	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv1827111	chr1:152472839-152690073	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv1830764	chr1:152472839-152690073	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv2757755	chr1:152472839-152898153	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	esv2758970	chr1:152472839-152898153	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	esv33483	chr1:152550269-152775526	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv547891	chr1:152556085-152770446	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv469873	chr1:152563260-152713616	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv482518	chr1:152563260-152713616	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv1001647	chr1:152572876-152678509	Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv427786	chr1:152572990-152898153	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
12	nsv1013433	chr1:152619305-153262215	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
13	nsv535170	chr1:152619305-153262215	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
14	nsv1005047	chr1:152636316-152656590	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	esv3382870	chr1:152641788-152653697	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	esv3335832	chr1:152647330-152658158	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
17	esv3352073	chr1:152647628-152659726	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
18	esv3448512	chr1:152647728-152660526	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
19	esv2764247	chr1:152647912-152661380	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
20	esv3409331	chr1:152648017-152658911	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
21	esv3453714	chr1:152648170-152659109	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
22	esv3453715	chr1:152648170-152659109	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
23	nsv8424	chr1:152648237-152658957	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
24	nsv947324	chr1:152648442-152658513	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
25	nsv1001834	chr1:152648853-153279143	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
26	esv20569	chr1:152648867-152660425	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
27	nsv441715	chr1:152649112-152656542	Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
28	nsv514008	chr1:152649888-152655744	Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152652800-152654400	Enhancers	Fetal Brain Male	brain

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