Variant report

Variant	rs61621249
Chromosome Location	chr6:150421278-150421279
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150420929..150422703-chr6:150428326..150430256,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1953321	0.81[EUR][1000 genomes]
rs2343533	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35063891	0.81[EUR][1000 genomes]
rs4869827	0.82[ASN][1000 genomes]
rs4870300	0.81[ASN][1000 genomes]
rs57363122	0.84[ASN][1000 genomes]
rs59567523	0.81[EUR][1000 genomes]
rs60091146	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60169056	0.81[ASN][1000 genomes]
rs6931545	0.81[EUR][1000 genomes]
rs6931571	0.81[EUR][1000 genomes]
rs6932103	0.81[EUR][1000 genomes]
rs6940563	0.81[EUR][1000 genomes]
rs73603909	0.81[EUR][1000 genomes]
rs736065	0.82[ASN][1000 genomes]
rs7761921	0.81[EUR][1000 genomes]
rs7769307	0.81[EUR][1000 genomes]
rs7769319	0.81[EUR][1000 genomes]
rs7773817	0.81[EUR][1000 genomes]
rs7774282	0.81[EUR][1000 genomes]
rs7774298	0.81[EUR][1000 genomes]
rs9479640	0.81[EUR][1000 genomes]
rs9479648	0.81[EUR][1000 genomes]
rs9479683	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9791221	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv886770	chr6:150395424-150499889	Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1016239	chr6:150407607-150424171	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv1024915	chr6:150407607-150425510	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv886771	chr6:150411442-150437749	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2763601	chr6:150412587-150425522	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1026690	chr6:150419115-150485583	Bivalent Enhancer Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150410400-150421800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:150420800-150421800	Bivalent Enhancer	K562	blood

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