Variant report

Variant	rs35850913
Chromosome Location	chr3:100775080-100775081
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10511182	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13059867	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13060849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13065583	0.83[EUR][1000 genomes]
rs13065684	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13074729	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13081830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13085636	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13085839	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13086519	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16843198	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16843216	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16843225	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16843229	0.93[EUR][1000 genomes]
rs17219986	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1839298	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs34281790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35252712	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs35333915	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35337386	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs35573711	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs35856427	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35974360	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs36077661	0.83[EUR][1000 genomes]
rs36082674	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs41386544	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs58427219	0.82[EUR][1000 genomes]
rs62274066	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62274067	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62274076	0.83[EUR][1000 genomes]
rs62274077	0.83[EUR][1000 genomes]
rs62274078	0.83[EUR][1000 genomes]
rs62275774	0.87[AMR][1000 genomes]
rs62275825	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs62275826	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs66598219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67144487	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931417	chr3:100547347-101183844	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	esv2757881	chr3:100613387-100776497	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2759163	chr3:100613387-100776497	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv877222	chr3:100715576-101038297	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv591176	chr3:100763611-100799644	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv591177	chr3:100767398-100799644	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3344837	chr3:100774311-100789597	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100762600-100780200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links