Variant report

Variant	rs62170337
Chromosome Location	chr2:77172592-77172593
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10520177	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1075716	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1077111	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11901979	0.89[EUR][1000 genomes]
rs13388459	0.90[ASN][1000 genomes]
rs13413951	0.90[ASN][1000 genomes]
rs1446721	0.81[AMR][1000 genomes]
rs17333578	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17333696	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17333850	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17333926	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17334205	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17334240	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17334254	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17334261	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17405724	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17405864	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17405905	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17405953	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs17405981	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17406023	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17406091	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17406146	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17406202	0.88[ASN][1000 genomes]
rs1929454	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4396752	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4401235	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4447628	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4491748	0.80[EUR][1000 genomes]
rs4637153	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62170208	0.90[ASN][1000 genomes]
rs62170210	0.90[ASN][1000 genomes]
rs62170328	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62170329	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62170330	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62170331	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62170332	0.94[EUR][1000 genomes]
rs62170336	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62170339	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62170864	0.90[ASN][1000 genomes]
rs62170865	0.88[ASN][1000 genomes]
rs62170866	0.88[ASN][1000 genomes]
rs62171961	0.82[AMR][1000 genomes]
rs62171964	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62171994	0.90[ASN][1000 genomes]
rs62171995	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62171996	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62171997	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66769122	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6742824	0.90[ASN][1000 genomes]
rs72823112	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72823135	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823137	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823174	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823182	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823183	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs953855	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874322	chr2:77031247-77209750	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv2752990	chr2:77038541-77217310	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv874324	chr2:77048896-77201916	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv874327	chr2:77085752-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv874328	chr2:77096124-77196122	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv874329	chr2:77096124-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv874330	chr2:77103719-77209750	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	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
9	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77172200-77174600	Enhancers	Fetal Lung	lung

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