Variant report

Variant	rs73956436
Chromosome Location	chr2:111522868-111522869
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	chr2:111521418..111524009-chr2:111524992..111527705,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs55693530	0.97[AFR][1000 genomes]
rs55928449	0.87[AFR][1000 genomes]
rs56019085	0.82[AFR][1000 genomes]
rs56238232	0.90[AFR][1000 genomes]
rs57166069	0.97[AFR][1000 genomes]
rs57431143	0.82[AFR][1000 genomes]
rs57934984	0.83[AFR][1000 genomes]
rs58796451	0.83[AFR][1000 genomes]
rs59952084	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61203060	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61392982	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72828851	0.81[AFR][1000 genomes]
rs73954660	0.93[AFR][1000 genomes]
rs73954668	0.90[AFR][1000 genomes]
rs73954672	0.97[AFR][1000 genomes]
rs73956432	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956434	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956437	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956438	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956439	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956441	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73956443	0.90[AFR][1000 genomes]
rs73956446	0.85[AFR][1000 genomes]
rs73956448	0.87[AFR][1000 genomes]
rs73956449	0.90[AFR][1000 genomes]
rs73956450	1.00[AFR][1000 genomes]
rs73956451	1.00[AFR][1000 genomes]
rs73956453	0.90[AFR][1000 genomes]
rs73956454	0.90[AFR][1000 genomes]
rs73956455	0.84[AFR][1000 genomes]
rs73956457	0.83[AFR][1000 genomes]
rs73956458	0.83[AFR][1000 genomes]
rs73956459	0.83[AFR][1000 genomes]
rs73956460	0.90[AFR][1000 genomes]
rs73956461	0.90[AFR][1000 genomes]
rs73956467	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1008758	chr2:111415136-111626467	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv535890	chr2:111415136-111626467	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv997829	chr2:111486961-111780537	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr2:111513200-111525800	Weak transcription	Fetal Heart	heart
2	chr2:111517400-111524400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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