Variant report

Variant	rs2732462
Chromosome Location	chr12:48696384-48696385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:48695552..48697163-chr12:48743180..48744695,2	K562	blood:
2	chr12:48695827..48697706-chr12:48743436..48745025,2	K562	blood:
3	chr12:48689964..48692021-chr12:48694764..48697453,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257735	Chromatin interaction
ENSG00000167528	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1061986	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1107654	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11168460	0.83[EUR][1000 genomes]
rs11168464	0.85[EUR][1000 genomes]
rs11168468	0.90[EUR][1000 genomes]
rs11168474	0.90[EUR][1000 genomes]
rs11168484	0.92[EUR][1000 genomes]
rs12828309	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12829841	0.92[EUR][1000 genomes]
rs1387259	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1387260	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1489108	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1542707	0.92[EUR][1000 genomes]
rs1552550	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2054905	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2409003	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2409004	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2450994	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2450996	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2468943	0.83[EUR][1000 genomes]
rs2468949	0.82[EUR][1000 genomes]
rs2634676	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2634678	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2634680	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2634681	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2634682	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2634684	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2634686	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2634688	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2634689	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2634691	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2634692	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2634693	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2634694	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2732441	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2732448	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2732453	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2732454	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2732457	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2732461	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2732466	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2732479	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2732481	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2732484	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2732486	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2956703	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2956710	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34286639	0.92[EUR][1000 genomes]
rs6580662	0.91[EUR][1000 genomes]
rs7297824	0.83[EUR][1000 genomes]
rs7307566	0.88[EUR][1000 genomes]
rs7315820	0.83[EUR][1000 genomes]
rs7966829	0.90[EUR][1000 genomes]
rs923397	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv8971	chr12:48536526-48758501	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv34439	chr12:48541757-48779562	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	esv2757502	chr12:48547128-48779562	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv899062	chr12:48658212-48711867	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv899063	chr12:48664989-48713768	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv899064	chr12:48664989-48721832	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv899065	chr12:48667019-48711867	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
10	nsv899066	chr12:48667019-48713768	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv427911	chr12:48670336-48979396	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
12	esv34952	chr12:48672333-48703533	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv469369	chr12:48675783-48711867	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv469370	chr12:48675783-48711867	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv469372	chr12:48675783-48711867	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
16	nsv470290	chr12:48675783-48711867	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv558791	chr12:48675783-48711867	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv832402	chr12:48686761-48851020	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
19	nsv826362	chr12:48693048-48768853	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2732462	H1FNT	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48694800-48696800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:48696200-48696600	Enhancers	Primary monocytes fromperipheralblood	blood

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