Variant report

Variant	rs55929632
Chromosome Location	chr5:35951111-35951112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10044791	1.00[AMR][1000 genomes]
rs10056322	1.00[AMR][1000 genomes]
rs55706410	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56392607	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61710272	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73092050	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73748710	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750046	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750049	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750058	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750059	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7701176	0.84[AFR][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	nsv471011	chr5:35861068-36003217	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830261	chr5:35863084-36018048	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1025695	chr5:35902486-36036934	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr5:35949800-35952000	Weak transcription	Liver	Liver
2	chr5:35950800-35953600	Weak transcription	Fetal Intestine Small	intestine
3	chr5:35950800-35953800	Weak transcription	Fetal Intestine Large	intestine

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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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