Variant report

Variant	rs12059823
Chromosome Location	chr1:103711531-103711532
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:72)

rs_ID	r²[population]
rs10437032	1.00[AMR][1000 genomes]
rs10493994	1.00[AMR][1000 genomes]
rs11164724	1.00[AMR][1000 genomes]
rs11164725	1.00[AMR][1000 genomes]
rs11164730	1.00[AMR][1000 genomes]
rs11164731	1.00[AMR][1000 genomes]
rs11164733	1.00[AMR][1000 genomes]
rs11164735	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11164736	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11164737	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11164738	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11164739	0.88[AFR][1000 genomes]
rs11164751	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11164752	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12059958	1.00[AMR][1000 genomes]
rs12060328	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12060714	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12061112	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12061317	1.00[AMR][1000 genomes]
rs12062539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12062593	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12068683	1.00[AMR][1000 genomes]
rs12072826	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12072971	1.00[AMR][1000 genomes]
rs12074606	1.00[AMR][1000 genomes]
rs12077747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12078453	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12082997	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12085205	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12096208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12098060	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12098103	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12239554	1.00[AMR][1000 genomes]
rs12240156	1.00[AMR][1000 genomes]
rs13374130	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1609258	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17127638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17127642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17127659	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28469637	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28630865	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55687112	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56086106	1.00[AMR][1000 genomes]
rs56219021	1.00[AMR][1000 genomes]
rs56914812	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57781890	1.00[AMR][1000 genomes]
rs58011743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58942206	1.00[AMR][1000 genomes]
rs58952834	1.00[AMR][1000 genomes]
rs58982700	1.00[AMR][1000 genomes]
rs59799567	1.00[AMR][1000 genomes]
rs61543247	1.00[AMR][1000 genomes]
rs61595551	1.00[AMR][1000 genomes]
rs61708772	1.00[AMR][1000 genomes]
rs72993115	1.00[AMR][1000 genomes]
rs72993118	1.00[AMR][1000 genomes]
rs72993177	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993190	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993197	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993201	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993202	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995206	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995208	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995209	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74108610	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74108618	0.85[AFR][1000 genomes]
rs74110906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74110911	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74110912	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74110913	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111525	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv931600	chr1:103548397-104161031	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv498007	chr1:103573857-104107589	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv432554	chr1:103673437-104128773	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr1:103710800-103712800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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