Variant report

Variant	rs1596739
Chromosome Location	chr11:85633368-85633369
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10128700	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10501603	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10501605	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10501607	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11234489	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11234492	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11234496	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11234502	0.90[EUR][1000 genomes]
rs11234512	0.90[EUR][1000 genomes]
rs11234513	0.90[EUR][1000 genomes]
rs11234517	0.90[EUR][1000 genomes]
rs12270433	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12278260	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12279956	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12281958	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12282655	0.83[EUR][1000 genomes]
rs12287170	0.90[EUR][1000 genomes]
rs17744938	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17745105	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17745153	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17745236	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17745248	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17745273	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17817582	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17817588	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17817690	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17817859	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17817883	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17817919	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17817956	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2001241	0.83[EUR][1000 genomes]
rs2084077	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs41381550	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4943934	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4943936	0.85[AMR][1000 genomes]
rs4944550	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4944551	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4944552	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4944553	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4944554	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4944555	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55697624	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55791429	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55815523	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56026701	0.86[EUR][1000 genomes]
rs56187740	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs57125313	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58937798	0.86[EUR][1000 genomes]
rs60185300	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72947601	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72949419	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72949429	0.87[AMR][1000 genomes]
rs72949443	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72950443	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72950453	0.83[EUR][1000 genomes]
rs72950456	0.83[EUR][1000 genomes]
rs72951266	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72951268	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72959177	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72959197	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72961110	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72961111	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72963077	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72963086	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72963092	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72965157	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72965166	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7927222	0.83[AMR][1000 genomes];0.83[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	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv1035489	chr11:85502953-85778229	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1048818	chr11:85524635-85746473	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv541116	chr11:85524635-85746473	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv898053	chr11:85579304-85634425	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1053808	chr11:85588919-85757693	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr11:85630200-85633400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr11:85630600-85637600	Enhancers	HepG2	liver

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