Variant report

Variant	rs17436410
Chromosome Location	chr7:26994167-26994168
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10227231	0.81[ASN][1000 genomes]
rs10227529	0.81[ASN][1000 genomes]
rs10227553	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10227673	0.81[ASN][1000 genomes]
rs10236221	0.81[ASN][1000 genomes]
rs10238645	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10242572	0.81[ASN][1000 genomes]
rs10244751	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10248500	0.81[ASN][1000 genomes]
rs10248684	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10251839	0.81[ASN][1000 genomes]
rs10256250	0.81[ASN][1000 genomes]
rs10270187	0.81[ASN][1000 genomes]
rs10272190	0.81[ASN][1000 genomes]
rs10272457	0.81[ASN][1000 genomes]
rs10272603	0.81[ASN][1000 genomes]
rs10486483	0.81[ASN][1000 genomes]
rs10486485	0.83[ASN][1000 genomes]
rs11563327	0.87[AMR][1000 genomes]
rs12530718	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12533561	0.84[ASN][1000 genomes]
rs12534899	0.81[ASN][1000 genomes]
rs12534901	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12534912	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12534921	0.81[ASN][1000 genomes]
rs12535784	0.81[ASN][1000 genomes]
rs12536145	0.81[ASN][1000 genomes]
rs12540045	0.81[ASN][1000 genomes]
rs12540388	0.83[ASN][1000 genomes]
rs12540508	0.81[ASN][1000 genomes]
rs13438514	0.81[ASN][1000 genomes]
rs17315929	0.81[ASN][1000 genomes]
rs17323934	0.83[ASN][1000 genomes]
rs17375272	0.81[ASN][1000 genomes]
rs17376018	0.81[ASN][1000 genomes]
rs17377696	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17471061	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17471088	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1967332	0.81[ASN][1000 genomes]
rs1982995	0.81[ASN][1000 genomes]
rs2031811	0.81[ASN][1000 genomes]
rs2253415	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2254463	0.83[ASN][1000 genomes]
rs2264802	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2264803	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2391362	0.83[ASN][1000 genomes]
rs2428416	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2428417	0.82[AMR][1000 genomes]
rs2428421	0.82[AMR][1000 genomes]
rs2462900	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2462902	0.83[ASN][1000 genomes]
rs2462904	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2462910	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465264	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2465266	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2465271	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465274	0.80[AMR][1000 genomes]
rs2522824	0.83[ASN][1000 genomes]
rs2648076	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2693659	0.82[AMR][1000 genomes]
rs2693662	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2693665	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2693668	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2712238	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2712242	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2712244	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2712245	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2712246	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28550029	0.81[ASN][1000 genomes]
rs28816386	0.81[ASN][1000 genomes]
rs28883078	0.81[ASN][1000 genomes]
rs3213853	0.81[ASN][1000 genomes]
rs3801803	0.83[ASN][1000 genomes]
rs3801805	0.81[ASN][1000 genomes]
rs3801807	0.81[ASN][1000 genomes]
rs3801808	0.81[ASN][1000 genomes]
rs3801809	0.81[ASN][1000 genomes]
rs3801812	0.81[ASN][1000 genomes]
rs3801813	0.81[ASN][1000 genomes]
rs3801814	0.81[ASN][1000 genomes]
rs3801815	0.81[ASN][1000 genomes]
rs3801819	0.81[ASN][1000 genomes]
rs3823928	0.81[ASN][1000 genomes]
rs3934268	0.81[ASN][1000 genomes]
rs4719882	0.81[ASN][1000 genomes]
rs4722647	0.81[ASN][1000 genomes]
rs55889667	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56144845	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56154570	0.81[ASN][1000 genomes]
rs57623217	0.81[ASN][1000 genomes]
rs59254259	0.81[ASN][1000 genomes]
rs61354389	0.81[ASN][1000 genomes]
rs62454249	0.91[ASN][1000 genomes]
rs6461979	0.81[ASN][1000 genomes]
rs6461980	0.81[ASN][1000 genomes]
rs73069507	0.81[ASN][1000 genomes]
rs73069510	0.81[ASN][1000 genomes]
rs73069533	0.81[ASN][1000 genomes]
rs73069540	0.83[ASN][1000 genomes]
rs73069541	0.83[ASN][1000 genomes]
rs7791513	0.81[ASN][1000 genomes]
rs7804356	0.81[ASN][1000 genomes]
rs7804620	0.81[ASN][1000 genomes]
rs7805766	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1033272	chr7:26976426-27020206	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17436410	HOXA2	cis	Whole Blood	GTEx

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26985200-26994600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:26991200-26998000	Weak transcription	NHDF-Ad	bronchial
3	chr7:26991600-26999200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:26992000-26994400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:26992200-26994800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:26992600-26994600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:26992800-26994400	Weak transcription	Fetal Lung	lung
8	chr7:26993000-26994400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:26993000-26994400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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