Variant report

Variant	rs4267743
Chromosome Location	chr4:133222560-133222561
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10007080	0.82[ASN][1000 genomes]
rs10007085	0.82[ASN][1000 genomes]
rs10029366	0.82[ASN][1000 genomes]
rs10212986	0.82[ASN][1000 genomes]
rs1039269	0.82[ASN][1000 genomes]
rs1039270	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12108519	0.96[ASN][1000 genomes]
rs12646539	0.94[ASN][1000 genomes]
rs12647149	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13126205	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13132555	0.81[ASN][1000 genomes]
rs1353839	0.81[ASN][1000 genomes]
rs1353840	0.83[ASN][1000 genomes]
rs1353841	0.83[ASN][1000 genomes]
rs1499322	0.83[ASN][1000 genomes]
rs1499323	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1499324	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1499328	0.83[ASN][1000 genomes]
rs1499337	0.83[ASN][1000 genomes]
rs1580809	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1827128	0.81[ASN][1000 genomes]
rs1846509	0.82[ASN][1000 genomes]
rs2648815	0.81[ASN][1000 genomes]
rs2648820	0.80[ASN][1000 genomes]
rs2657412	0.81[ASN][1000 genomes]
rs2657413	0.81[ASN][1000 genomes]
rs2657414	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2657423	0.81[ASN][1000 genomes]
rs2657424	0.81[ASN][1000 genomes]
rs28493696	0.83[ASN][1000 genomes]
rs28619296	0.83[ASN][1000 genomes]
rs28661998	0.83[ASN][1000 genomes]
rs28885387	0.83[ASN][1000 genomes]
rs4260556	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4371625	0.99[ASN][1000 genomes]
rs60224107	0.82[ASN][1000 genomes]
rs60968377	0.81[ASN][1000 genomes]
rs62317704	0.82[ASN][1000 genomes]
rs7667347	0.99[ASN][1000 genomes]
rs7667592	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7693391	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs904518	0.81[ASN][1000 genomes]
rs905897	0.81[ASN][1000 genomes]
rs9993946	0.88[ASN][1000 genomes]
rs9997674	0.82[ASN][1000 genomes]
rs9997695	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031888	chr4:132903485-133355824	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv595445	chr4:133022641-133338765	Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv880003	chr4:133047300-133513991	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv880004	chr4:133093090-133236522	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv880005	chr4:133101094-133233538	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2757955	chr4:133153860-133298149	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2759283	chr4:133153860-133298149	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv461645	chr4:133160255-133293122	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv595446	chr4:133160255-133293122	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv595447	chr4:133160737-133252054	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv880006	chr4:133160737-133278913	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv880007	chr4:133160737-133397984	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv880009	chr4:133164679-133233538	Enhancers ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
14	nsv880010	chr4:133165898-133236522	Enhancers Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
15	nsv880011	chr4:133165898-133278913	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv880012	chr4:133165898-133397984	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv880013	chr4:133165898-133461762	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv595448	chr4:133171171-133236522	ZNF genes & repeats Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
19	nsv880014	chr4:133171171-133236522	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
20	nsv880015	chr4:133176897-133236522	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
21	nsv880016	chr4:133176897-133257963	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv880017	chr4:133176897-133270056	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv880018	chr4:133176897-133278913	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv880019	chr4:133176897-133508970	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
25	nsv1015991	chr4:133185412-133224362	Enhancers ZNF genes & repeats Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
26	nsv880020	chr4:133187185-133461762	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
27	nsv880021	chr4:133189144-133278913	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv880022	chr4:133212878-133293122	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
29	nsv880023	chr4:133216564-133289007	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
30	nsv880024	chr4:133216564-133397984	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
31	nsv880025	chr4:133216564-133424752	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133222400-133222600	Enhancers	Fetal Lung	lung

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