Variant report

Variant	rs72787349
Chromosome Location	chr10:26384051-26384052
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10508713	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11014866	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11014874	0.86[EUR][1000 genomes]
rs11812370	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11816461	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11816664	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11817896	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16926590	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16926628	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16926660	0.85[AMR][1000 genomes]
rs17666893	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17667157	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs17739436	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17739453	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17739680	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2222351	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3897758	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs41279908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4370835	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56153367	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56234810	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57140603	0.85[AMR][1000 genomes]
rs57687518	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58309865	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59646929	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61284099	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6650135	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7070437	0.86[EUR][1000 genomes]
rs7074143	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7082557	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72787350	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72789947	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72789954	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72789957	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72789960	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72793209	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72793210	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72793214	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72793215	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72793218	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72793939	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72793940	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72793945	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72793992	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs74126361	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs74126386	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74126397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74126400	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74126401	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74126402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74129103	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74129107	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74129109	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs74129112	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs74129113	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7894269	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7909349	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7919609	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26373400-26390400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26382200-26386600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links