Variant report

Variant	rs12426014
Chromosome Location	chr12:47145441-47145442
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10748451	0.80[EUR][1000 genomes]
rs10880996	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10880997	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11183575	0.83[ASN][1000 genomes]
rs11183576	0.83[ASN][1000 genomes]
rs11183600	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11610453	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11830275	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12423908	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12426320	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12426545	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12426593	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12823568	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs180403	0.87[CHB][hapmap]
rs180405	0.87[CHB][hapmap]
rs180408	0.87[CHB][hapmap]
rs180409	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs180410	0.87[CHB][hapmap]
rs180412	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs180415	0.84[CHB][hapmap]
rs180417	0.84[CHB][hapmap]
rs180421	0.83[CHB][hapmap]
rs180423	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs180427	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs180428	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs180429	0.83[CHB][hapmap]
rs180430	0.83[CHB][hapmap]
rs2080687	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2080689	0.81[ASN][1000 genomes]
rs2098512	0.84[EUR][1000 genomes]
rs2111772	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2287467	0.82[EUR][1000 genomes]
rs2408622	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2408623	0.81[ASN][1000 genomes]
rs2430916	0.80[ASN][1000 genomes]
rs2430921	0.87[CHB][hapmap]
rs2465582	0.87[CHB][hapmap]
rs2465584	0.87[CHB][hapmap]
rs2543334	0.81[ASN][1000 genomes]
rs2715783	0.81[ASN][1000 genomes]
rs35813765	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs35827448	0.89[ASN][1000 genomes]
rs4140781	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4140782	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7300739	0.82[EUR][1000 genomes]
rs7316285	0.81[ASN][1000 genomes]
rs7484804	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7484950	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7959022	0.82[EUR][1000 genomes]
rs7972141	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv3416674	chr12:46988689-47178369	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv3374922	chr12:47144185-47145733	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47145200-47145600	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr12:47145200-47146200	Weak transcription	Primary T cells from cord blood	blood
3	chr12:47145200-47146200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr12:47145200-47146400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr12:47145200-47146800	Enhancers	HepG2	liver

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