Variant report

Variant	rs73067906
Chromosome Location	chr5:27388089-27388090
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:27386479..27389149-chr5:27394969..27398145,3	K562	blood:
2	chr5:27384539..27388630-chr5:27389237..27391656,3	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10058813	1.00[EUR][1000 genomes]
rs12153780	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12188151	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1382909	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16896634	0.93[EUR][1000 genomes]
rs16896639	0.97[EUR][1000 genomes]
rs16896645	0.97[EUR][1000 genomes]
rs16896651	0.97[EUR][1000 genomes]
rs16896657	0.97[EUR][1000 genomes]
rs16896665	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16896676	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16899573	0.93[EUR][1000 genomes]
rs1993951	0.97[EUR][1000 genomes]
rs1993952	0.97[EUR][1000 genomes]
rs34502	1.00[EUR][1000 genomes]
rs3846563	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3966086	0.97[EUR][1000 genomes]
rs4367261	0.97[EUR][1000 genomes]
rs73065921	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73065935	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73065948	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73067936	0.86[AFR][1000 genomes]
rs73746095	0.86[EUR][1000 genomes]
rs73746096	0.90[EUR][1000 genomes]
rs73746097	0.97[EUR][1000 genomes]
rs73746098	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73746099	0.97[EUR][1000 genomes]
rs73746100	0.90[EUR][1000 genomes]
rs7701855	0.97[EUR][1000 genomes]
rs7716017	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7716845	0.97[EUR][1000 genomes]
rs7718306	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881286	chr5:27135351-27770554	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv880298	chr5:27193573-27659111	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv880326	chr5:27193573-27743375	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv880623	chr5:27279981-27559659	Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv880525	chr5:27308254-27447863	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1029060	chr5:27313831-27411288	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
7	nsv881318	chr5:27323746-27559659	Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv1034704	chr5:27324221-27410790	Enhancers Weak transcription Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv1022838	chr5:27324221-27411288	Enhancers Active TSS Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
10	nsv880317	chr5:27328631-27447863	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv881503	chr5:27344037-27510050	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	nsv881216	chr5:27361816-27464184	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv881475	chr5:27376682-27510050	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	nsv881003	chr5:27376682-27539490	Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv880935	chr5:27376682-27559659	Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	nsv880535	chr5:27376682-27706007	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv880631	chr5:27379706-27432346	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	nsv881089	chr5:27387385-27478198	ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:27387000-27389200	Enhancers	HepG2	liver
2	chr5:27387400-27388200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr5:27387600-27388200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:27387600-27388200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:27387600-27388200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:27387600-27388200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:27387600-27388800	Enhancers	HUES6 Cell Line	embryonic stem cell

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