Variant report

Variant	rs6042526
Chromosome Location	chr20:14074213-14074214
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs6033866	1.00[AMR][1000 genomes]
rs6033895	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6033899	1.00[AMR][1000 genomes]
rs6042472	1.00[AMR][1000 genomes]
rs6042477	1.00[AMR][1000 genomes]
rs6042480	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042502	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042551	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042557	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6042579	1.00[AMR][1000 genomes]
rs6042586	1.00[AMR][1000 genomes]
rs73255017	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066810	chr20:13451869-14432454	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv912689	chr20:13570331-14155881	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv531479	chr20:13632491-14434432	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv585438	chr20:14054163-14171905	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14066000-14074400	Weak transcription	Ovary	ovary
2	chr20:14073800-14075400	Enhancers	Stomach Mucosa	stomach
3	chr20:14074200-14075000	Active TSS	Pancreatic Islets	Pancreatic Islet

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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