Variant report

Variant	rs72671675
Chromosome Location	chr1:67333064-67333065
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12239035	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12239074	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1280338	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1925399	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1925400	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1925401	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1925402	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1925403	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1925404	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1925405	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1925406	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1931297	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2147835	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs269395	0.81[EUR][1000 genomes]
rs269399	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs269401	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs269402	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs269403	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs269405	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2991353	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2991354	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2991359	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4255358	0.82[EUR][1000 genomes]
rs55858354	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56400880	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs573490	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61467716	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6699606	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72671671	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72671673	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72671674	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72671677	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72671679	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72671680	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72671682	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72671685	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7552770	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869413	chr1:67082512-67414286	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv830093	chr1:67173594-67348264	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv546443	chr1:67268642-67352960	Genic enhancers Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv871738	chr1:67268642-67375206	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv871259	chr1:67275027-67375206	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67276800-67336000	Weak transcription	Aorta	Aorta
2	chr1:67281600-67335800	Weak transcription	Ovary	ovary
3	chr1:67319400-67335400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:67329800-67335000	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links