Variant report

Variant	rs2464521
Chromosome Location	chr4:89814915-89814916
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10001420	0.87[ASN][1000 genomes]
rs10019862	0.92[ASN][1000 genomes]
rs10028121	0.92[ASN][1000 genomes]
rs10033435	0.88[ASN][1000 genomes]
rs10033476	0.88[ASN][1000 genomes]
rs1246630	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1246633	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1246637	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1246638	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1246639	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1246641	0.96[ASN][1000 genomes]
rs1272570	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13106968	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13148439	0.92[ASN][1000 genomes]
rs1355836	0.80[ASN][1000 genomes]
rs1355837	0.80[ASN][1000 genomes]
rs1398937	0.80[ASN][1000 genomes]
rs1398938	0.87[ASN][1000 genomes]
rs1398939	0.87[ASN][1000 genomes]
rs1398941	0.87[ASN][1000 genomes]
rs1398943	0.80[ASN][1000 genomes]
rs1458552	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1458553	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1458555	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1513811	0.80[ASN][1000 genomes]
rs1513812	0.80[ASN][1000 genomes]
rs1513823	0.80[ASN][1000 genomes]
rs1533289	0.80[ASN][1000 genomes]
rs1708659	0.80[ASN][1000 genomes]
rs1708671	0.84[ASN][1000 genomes]
rs1708672	0.84[ASN][1000 genomes]
rs1708673	0.80[ASN][1000 genomes]
rs1708683	0.80[ASN][1000 genomes]
rs1795730	0.87[ASN][1000 genomes]
rs1795735	0.84[ASN][1000 genomes]
rs1795737	0.87[ASN][1000 genomes]
rs1795740	0.87[ASN][1000 genomes]
rs1828735	0.80[ASN][1000 genomes]
rs1903004	0.92[ASN][1000 genomes]
rs1903009	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1996139	0.80[ASN][1000 genomes]
rs2045516	0.96[ASN][1000 genomes]
rs2125410	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2446295	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2446302	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2446309	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2464511	0.87[ASN][1000 genomes]
rs2464526	0.92[ASN][1000 genomes]
rs2609254	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2609263	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2609266	0.92[ASN][1000 genomes]
rs2609274	0.96[ASN][1000 genomes]
rs2609278	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2609281	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2609284	0.88[ASN][1000 genomes]
rs2670618	0.80[ASN][1000 genomes]
rs2670619	0.87[ASN][1000 genomes]
rs2670620	0.87[ASN][1000 genomes]
rs2670627	0.80[ASN][1000 genomes]
rs2670628	0.80[ASN][1000 genomes]
rs2704572	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2704580	0.84[ASN][1000 genomes]
rs2704585	0.80[ASN][1000 genomes]
rs2704588	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2704591	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2704592	0.80[ASN][1000 genomes]
rs2704593	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2704602	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2704603	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2704606	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28559811	0.87[ASN][1000 genomes]
rs28624770	0.92[ASN][1000 genomes]
rs28658282	0.92[ASN][1000 genomes]
rs2869965	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2869968	0.96[ASN][1000 genomes]
rs28718401	0.80[ASN][1000 genomes]
rs28869547	0.87[ASN][1000 genomes]
rs4498109	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59698155	0.92[ASN][1000 genomes]
rs6532100	0.80[ASN][1000 genomes]
rs6834297	0.80[ASN][1000 genomes]
rs7673427	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7697878	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8180333	0.80[ASN][1000 genomes]
rs922027	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs938265	0.80[ASN][1000 genomes]
rs973680	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs987314	0.96[ASN][1000 genomes]
rs993358	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9999793	0.87[ASN][1000 genomes]
rs9999873	0.87[ASN][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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009354	chr4:89725914-89985155	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv998651	chr4:89800245-89933445	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv537175	chr4:89800245-89933445	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv879532	chr4:89811195-89917135	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:89802200-89820600	Weak transcription	Aorta	Aorta
2	chr4:89802600-89825600	Weak transcription	Ovary	ovary
3	chr4:89805400-89817600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:89809200-89828800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:89813400-89821400	Weak transcription	Fetal Intestine Small	intestine
6	chr4:89814400-89815200	Enhancers	Placenta	Placenta

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