Variant report

Variant	rs408127
Chromosome Location	chr5:111698164-111698165
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1004383	0.89[ASN][1000 genomes]
rs1004385	0.89[ASN][1000 genomes]
rs10052915	0.90[ASN][1000 genomes]
rs1019743	0.89[ASN][1000 genomes]
rs1019744	0.89[ASN][1000 genomes]
rs12519600	0.89[ASN][1000 genomes]
rs1474360	0.89[ASN][1000 genomes]
rs1962305	0.80[ASN][1000 genomes]
rs1975017	0.89[ASN][1000 genomes]
rs2042884	0.82[ASN][1000 genomes]
rs2140625	0.90[ASN][1000 genomes]
rs2140626	0.80[ASN][1000 genomes]
rs2416283	0.90[ASN][1000 genomes]
rs2416284	0.90[ASN][1000 genomes]
rs2839826	0.82[ASN][1000 genomes]
rs366217	0.93[ASN][1000 genomes]
rs366951	0.93[ASN][1000 genomes]
rs367807	0.92[ASN][1000 genomes]
rs368032	0.94[ASN][1000 genomes]
rs370640	0.93[ASN][1000 genomes]
rs373303	0.88[ASN][1000 genomes]
rs373583	0.92[ASN][1000 genomes]
rs376395	0.91[ASN][1000 genomes]
rs378791	0.81[ASN][1000 genomes]
rs382482	0.93[ASN][1000 genomes]
rs387117	0.92[ASN][1000 genomes]
rs388091	0.87[ASN][1000 genomes]
rs393096	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs406359	0.91[ASN][1000 genomes]
rs406444	0.91[ASN][1000 genomes]
rs408076	0.81[ASN][1000 genomes]
rs424998	0.91[ASN][1000 genomes]
rs429580	0.95[ASN][1000 genomes]
rs440759	0.90[ASN][1000 genomes]
rs441563	0.88[ASN][1000 genomes]
rs442777	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs442947	0.93[ASN][1000 genomes]
rs443024	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs447144	0.91[ASN][1000 genomes]
rs454794	0.90[ASN][1000 genomes]
rs4958040	0.89[ASN][1000 genomes]
rs6594591	0.91[ASN][1000 genomes]
rs6861186	0.87[ASN][1000 genomes]
rs6872155	0.81[ASN][1000 genomes]
rs6877695	0.89[ASN][1000 genomes]
rs7711318	0.89[ASN][1000 genomes]
rs7720180	0.88[ASN][1000 genomes]
rs7720546	0.88[ASN][1000 genomes]
rs7731169	0.80[ASN][1000 genomes]
rs821733	0.86[ASN][1000 genomes]
rs821734	0.86[ASN][1000 genomes]
rs821735	0.86[ASN][1000 genomes]
rs821745	0.86[ASN][1000 genomes]
rs987764	0.89[ASN][1000 genomes]
rs987765	0.83[AFR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015302	chr5:111339022-111802947	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv537861	chr5:111339022-111802947	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv599368	chr5:111399885-112032675	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv531291	chr5:111497440-111756788	Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv882714	chr5:111655382-111807579	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv462386	chr5:111667572-111699317	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv599372	chr5:111667572-111699317	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	esv3362916	chr5:111698082-111698275	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111684000-111702600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:111685200-111707000	Weak transcription	Ovary	ovary
3	chr5:111685200-111709800	Weak transcription	Aorta	Aorta
4	chr5:111689200-111702200	Weak transcription	Gastric	stomach
5	chr5:111689600-111708800	Weak transcription	Esophagus	oesophagus
6	chr5:111693800-111703200	Weak transcription	Right Ventricle	heart
7	chr5:111694000-111700800	Weak transcription	Left Ventricle	heart
8	chr5:111694000-111701800	Weak transcription	Right Atrium	heart

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