Variant report

Variant	rs28718441
Chromosome Location	chr4:21089200-21089201
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10007120	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10028465	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10028561	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10029228	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11944192	0.81[ASN][1000 genomes]
rs12642991	0.84[ASN][1000 genomes]
rs12643371	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12646516	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12649352	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12649359	0.82[ASN][1000 genomes]
rs1433493	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1560786	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1560788	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1560790	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16870421	0.84[ASN][1000 genomes]
rs1897664	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28390301	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28396704	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28492736	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59916150	0.80[EUR][1000 genomes]
rs61277470	0.84[ASN][1000 genomes]
rs6448011	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6448013	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6448016	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6448018	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6448019	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6814358	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6824763	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7356370	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7356371	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7667541	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7673495	0.84[ASN][1000 genomes]
rs7688396	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7689134	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7689193	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7689340	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7694857	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7695039	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7696887	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv829878	chr4:20966047-21138626	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv878745	chr4:21054348-21155716	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv878746	chr4:21054348-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv878747	chr4:21057794-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv522328	chr4:21083553-21096827	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21085800-21089800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:21086000-21089600	Weak transcription	HUVEC	blood vessel

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