Variant report

Variant	rs72823176
Chromosome Location	chr2:77227269-77227270
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10172981	0.88[EUR][1000 genomes]
rs10208087	0.91[EUR][1000 genomes]
rs10520177	0.96[EUR][1000 genomes]
rs1075716	0.96[EUR][1000 genomes]
rs1077111	0.96[EUR][1000 genomes]
rs11901979	0.85[ASN][1000 genomes]
rs13388459	0.93[EUR][1000 genomes]
rs13413951	0.93[EUR][1000 genomes]
rs1345137	0.90[EUR][1000 genomes]
rs1446708	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1446721	0.95[EUR][1000 genomes]
rs17013567	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17013635	0.93[EUR][1000 genomes]
rs17333926	0.92[EUR][1000 genomes]
rs17334205	0.96[EUR][1000 genomes]
rs17334240	0.96[EUR][1000 genomes]
rs17334254	0.96[EUR][1000 genomes]
rs17334261	0.96[EUR][1000 genomes]
rs17334527	0.90[EUR][1000 genomes]
rs17405864	0.95[EUR][1000 genomes]
rs17405905	0.96[EUR][1000 genomes]
rs17405953	0.95[EUR][1000 genomes]
rs17405981	0.96[EUR][1000 genomes]
rs17406023	0.96[EUR][1000 genomes]
rs17406084	0.90[EUR][1000 genomes]
rs17406091	0.96[EUR][1000 genomes]
rs17406146	0.96[EUR][1000 genomes]
rs17406202	0.95[EUR][1000 genomes]
rs17406374	0.91[EUR][1000 genomes]
rs1960005	0.92[EUR][1000 genomes]
rs2077823	0.92[EUR][1000 genomes]
rs34007251	0.86[EUR][1000 genomes]
rs4396752	0.96[EUR][1000 genomes]
rs4401235	0.96[EUR][1000 genomes]
rs4447628	0.96[EUR][1000 genomes]
rs4491748	0.96[EUR][1000 genomes]
rs4637153	0.96[EUR][1000 genomes]
rs55800138	0.92[EUR][1000 genomes]
rs55864802	0.92[EUR][1000 genomes]
rs56055201	0.82[EUR][1000 genomes]
rs62170208	0.95[EUR][1000 genomes]
rs62170209	0.94[EUR][1000 genomes]
rs62170210	0.95[EUR][1000 genomes]
rs62170864	0.95[EUR][1000 genomes]
rs62170865	0.95[EUR][1000 genomes]
rs62170866	0.95[EUR][1000 genomes]
rs62170872	0.90[EUR][1000 genomes]
rs62170895	0.92[EUR][1000 genomes]
rs62170896	0.92[EUR][1000 genomes]
rs62170899	0.90[EUR][1000 genomes]
rs62170910	0.83[EUR][1000 genomes]
rs62170911	0.83[EUR][1000 genomes]
rs62170914	0.83[EUR][1000 genomes]
rs62170916	0.83[EUR][1000 genomes]
rs62170918	0.81[EUR][1000 genomes]
rs62171961	0.95[EUR][1000 genomes]
rs62171964	0.96[EUR][1000 genomes]
rs62171994	0.95[EUR][1000 genomes]
rs62171995	0.96[EUR][1000 genomes]
rs62171996	0.96[EUR][1000 genomes]
rs62171997	0.96[EUR][1000 genomes]
rs66769122	0.96[EUR][1000 genomes]
rs6742824	0.92[EUR][1000 genomes]
rs72823135	0.93[EUR][1000 genomes]
rs72823137	0.93[EUR][1000 genomes]
rs72823174	0.96[EUR][1000 genomes]
rs72823182	0.96[EUR][1000 genomes]
rs72823183	0.96[EUR][1000 genomes]
rs72823195	0.92[EUR][1000 genomes]
rs72823196	0.92[EUR][1000 genomes]
rs72823197	0.92[EUR][1000 genomes]
rs72825338	0.80[EUR][1000 genomes]
rs956657	0.92[EUR][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	nsv834266	chr2:77120236-77287504	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv949670	chr2:77125218-77712607	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv519950	chr2:77213103-77256291	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv961764	chr2:77216571-77228053	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77225000-77231400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:77226600-77227800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:77226800-77228600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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