Variant report

Variant	rs4886721
Chromosome Location	chr15:74168864-74168865
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11072448	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11636136	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12914677	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2084851	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4272992	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4445847	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4886717	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7163502	0.89[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr15:74167800-74169200	Enhancers	Fetal Intestine Large	intestine
2	chr15:74168200-74169200	Enhancers	Duodenum Mucosa	Duodenum
3	chr15:74168400-74170200	Weak transcription	Fetal Intestine Small	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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