Variant report

Variant	rs4325981
Chromosome Location	chr4:90024321-90024322
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:90023640..90025754-chr4:90032265..90034270,2	K562	blood:
2	chr4:90023640..90028371-chr4:90029997..90034270,7	K562	blood:

Variant related genes	Relation type
ENSG00000271359	Chromatin interaction
ENSG00000138640	Chromatin interaction
ENSG00000180346	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10433881	0.96[ASN][1000 genomes]
rs11734924	0.96[ASN][1000 genomes]
rs12645173	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12647095	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12649875	0.96[ASN][1000 genomes]
rs13105546	0.96[ASN][1000 genomes]
rs13133608	0.96[ASN][1000 genomes]
rs13138927	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1355836	0.85[ASN][1000 genomes]
rs1355837	0.85[ASN][1000 genomes]
rs1398937	0.85[ASN][1000 genomes]
rs1398943	0.85[ASN][1000 genomes]
rs1513811	0.85[ASN][1000 genomes]
rs1513812	0.85[ASN][1000 genomes]
rs1513823	0.85[ASN][1000 genomes]
rs1533288	0.82[ASN][1000 genomes]
rs1533289	0.85[ASN][1000 genomes]
rs1533294	0.93[ASN][1000 genomes]
rs1708659	0.85[ASN][1000 genomes]
rs1708671	0.81[ASN][1000 genomes]
rs1708672	0.81[ASN][1000 genomes]
rs1708683	0.85[ASN][1000 genomes]
rs1795735	0.81[ASN][1000 genomes]
rs1828735	0.85[ASN][1000 genomes]
rs1996139	0.85[ASN][1000 genomes]
rs2102650	0.93[ASN][1000 genomes]
rs2670618	0.85[ASN][1000 genomes]
rs2670627	0.85[ASN][1000 genomes]
rs2670628	0.85[ASN][1000 genomes]
rs2704580	0.81[ASN][1000 genomes]
rs2704585	0.85[ASN][1000 genomes]
rs2704592	0.85[ASN][1000 genomes]
rs2869989	0.93[ASN][1000 genomes]
rs28718401	0.85[ASN][1000 genomes]
rs2904264	0.93[ASN][1000 genomes]
rs4693985	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4693987	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532100	0.85[ASN][1000 genomes]
rs6532113	0.96[ASN][1000 genomes]
rs6823241	0.96[ASN][1000 genomes]
rs6826482	0.93[ASN][1000 genomes]
rs6834297	0.85[ASN][1000 genomes]
rs6843986	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6845264	0.93[ASN][1000 genomes]
rs6846010	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7657630	0.96[ASN][1000 genomes]
rs8180333	0.85[ASN][1000 genomes]
rs9307063	0.96[ASN][1000 genomes]
rs938265	0.85[ASN][1000 genomes]
rs938267	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv1007025	chr4:89837734-90098046	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537176	chr4:89837734-90098046	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1002448	chr4:89933385-90128133	Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90017200-90031600	Weak transcription	Right Atrium	heart
2	chr4:90021000-90029800	Weak transcription	Primary T cells from cord blood	blood
3	chr4:90023200-90026400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr4:90024200-90031800	Weak transcription	Aorta	Aorta

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