Variant report

Variant	rs4558192
Chromosome Location	chr11:5605899-5605900
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5600488..5604726-chr11:5605110..5607814,5	K562	blood:

Variant related genes	Relation type
ENSG00000187747	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10742718	0.81[EUR][1000 genomes]
rs10742719	0.81[EUR][1000 genomes]
rs10742720	0.81[EUR][1000 genomes]
rs10742721	0.81[EUR][1000 genomes]
rs10742722	0.81[EUR][1000 genomes]
rs10742723	0.81[EUR][1000 genomes]
rs10742725	0.81[EUR][1000 genomes]
rs10742726	0.81[EUR][1000 genomes]
rs10742729	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10742731	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10769074	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10769087	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10769088	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10769089	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10769092	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10769098	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10769101	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10838375	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10838377	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10838378	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10838379	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11038193	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2163946	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2341434	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4325336	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4547126	0.81[EUR][1000 genomes]
rs4550252	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4604918	0.81[EUR][1000 genomes]
rs4910572	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4910821	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4910822	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7927448	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7927677	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7929659	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7930588	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7930681	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7931917	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7942070	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs892336	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs967664	0.80[EUR][1000 genomes]
rs967665	0.81[EUR][1000 genomes]
rs967666	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048608	chr11:5328516-5645179	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
2	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv896939	chr11:5497799-5809548	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv553241	chr11:5506034-6203685	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
5	nsv896943	chr11:5583188-5619008	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1041568	chr11:5585716-5765688	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv896944	chr11:5588174-5625603	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv896945	chr11:5598864-5625603	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1054035	chr11:5604437-5620417	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	esv2760210	chr11:5604437-5620429	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5603000-5608400	Weak transcription	K562	blood

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