Variant report

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:46235668..46238517-chr11:46241557..46245176,4	K562	blood:
2	chr11:46243218..46244799-chr11:46411942..46414663,2	K562	blood:
3	chr11:46153781..46156284-chr11:46244392..46246290,2	K562	blood:
4	chr11:46241197..46245496-chr11:46256169..46258783,6	K562	blood:
5	chr11:46243733..46245784-chr11:46263716..46265600,2	K562	blood:
6	chr11:46243156..46245098-chr11:46255575..46258822,3	MCF-7	breast:
7	chr11:46240075..46247012-chr11:46255086..46262989,16	K562	blood:
8	chr11:46240364..46242725-chr11:46242954..46244645,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254639	Chromatin interaction
ENSG00000255269	Chromatin interaction

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10501317	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11605191	0.86[ASN][1000 genomes]
rs28755875	0.86[ASN][1000 genomes]
rs35671387	0.86[ASN][1000 genomes]
rs58301639	0.86[ASN][1000 genomes]
rs58678374	0.86[ASN][1000 genomes]
rs7104451	0.86[ASN][1000 genomes]
rs7113170	0.90[ASN][1000 genomes]
rs7116965	0.86[ASN][1000 genomes]
rs72908007	0.86[ASN][1000 genomes]
rs72908009	0.86[ASN][1000 genomes]
rs72908013	0.86[ASN][1000 genomes]
rs72908014	0.86[ASN][1000 genomes]
rs72908015	0.86[ASN][1000 genomes]
rs72908022	0.86[ASN][1000 genomes]
rs72908033	0.87[EUR][1000 genomes]
rs72908034	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72908050	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908052	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908065	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72908086	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72908091	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72908092	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72908096	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72908098	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72908102	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72910006	0.90[ASN][1000 genomes]
rs7926726	0.86[ASN][1000 genomes]
rs7931075	0.86[ASN][1000 genomes]
rs7943808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051344	chr11:46188818-46306447	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
2	nsv541028	chr11:46188818-46306447	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
3	nsv308	chr11:46242287-46287542	Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46244200-46244800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:46244200-46244800	Enhancers	Hela-S3	cervix
3	chr11:46244200-46245000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:46244400-46245000	Enhancers	HepG2	liver
5	chr11:46244400-46245400	Enhancers	Duodenum Mucosa	Duodenum
6	chr11:46244600-46245000	Enhancers	Fetal Intestine Small	intestine
7	chr11:46244600-46245000	Enhancers	Spleen	Spleen
8	chr11:46244600-46245400	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr11:46244600-46246000	Enhancers	K562	blood

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