Variant report

Variant	rs766120
Chromosome Location	chr5:164548126-164548127
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10076942	0.87[EUR][1000 genomes]
rs11135348	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1368423	0.88[CEU][hapmap]
rs1473186	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2052511	0.87[EUR][1000 genomes]
rs2112641	0.87[EUR][1000 genomes]
rs253536	0.91[EUR][1000 genomes]
rs2861088	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2861089	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2861093	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35142388	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35660522	0.87[EUR][1000 genomes]
rs4283809	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4382188	0.88[EUR][1000 genomes]
rs4489083	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4552632	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4563646	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4588611	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4591770	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6869716	0.89[EUR][1000 genomes]
rs6869965	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6896670	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7444721	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7447465	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs766122	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9314053	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs982305	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][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	nsv995060	chr5:163660200-164620500	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv528624	chr5:164319435-164701201	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1033866	chr5:164419608-164677758	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	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	chr5:164547400-164549400	Enhancers	Rectal Smooth Muscle	rectum
2	chr5:164547400-164549800	Enhancers	Fetal Lung	lung
3	chr5:164547600-164549400	Enhancers	Colon Smooth Muscle	Colon

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