Variant report

Variant	rs72823136
Chromosome Location	chr2:77203493-77203494
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10200209	0.81[ASN][1000 genomes]
rs10200557	0.81[ASN][1000 genomes]
rs10208262	0.93[AMR][1000 genomes]
rs1348832	0.88[ASN][1000 genomes]
rs1348833	0.88[ASN][1000 genomes]
rs1446716	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17013541	0.90[ASN][1000 genomes]
rs2028914	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58463979	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs59946045	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61145558	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs61391187	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72807245	0.86[EUR][1000 genomes]
rs72807251	0.86[EUR][1000 genomes]
rs72807256	0.86[EUR][1000 genomes]
rs72821245	0.81[ASN][1000 genomes]
rs72821297	0.93[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72821299	0.93[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72823111	0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72823116	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823138	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72823139	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72823141	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72823142	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72823144	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823152	0.90[ASN][1000 genomes]
rs72823157	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823158	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823159	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823168	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823173	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72823179	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7557841	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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	nsv874327	chr2:77085752-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv874329	chr2:77096124-77209750	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv874330	chr2:77103719-77209750	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	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
7	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
8	esv2756931	chr2:77185856-77209051	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2759066	chr2:77185856-77209051	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2762264	chr2:77202107-77206452	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77202600-77204200	Enhancers	HUVEC	blood vessel
2	chr2:77203000-77206600	Enhancers	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links