Variant report

Variant	rs10004804
Chromosome Location	chr4:97092719-97092720
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:97090606..97093234-chr4:97096848..97099825,3	K562	blood:
2	chr4:97090980..97093234-chr4:97096848..97099424,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10002816	0.80[ASN][1000 genomes]
rs10007900	0.87[EUR][1000 genomes]
rs10016180	0.96[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs10856919	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11942724	0.84[ASN][1000 genomes]
rs12499067	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12508802	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12509883	0.86[EUR][1000 genomes]
rs12642621	0.86[ASN][1000 genomes]
rs12650441	0.82[ASN][1000 genomes]
rs13104802	0.84[EUR][1000 genomes]
rs13150508	0.83[EUR][1000 genomes]
rs1354704	0.84[EUR][1000 genomes]
rs1373331	0.85[ASN][1000 genomes]
rs1395199	0.82[ASN][1000 genomes]
rs1425361	0.88[ASN][1000 genomes]
rs1506304	0.84[EUR][1000 genomes]
rs1506305	0.84[EUR][1000 genomes]
rs1506306	0.84[EUR][1000 genomes]
rs1506318	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1506321	0.81[ASN][1000 genomes]
rs1605227	0.84[EUR][1000 genomes]
rs1834360	0.88[ASN][1000 genomes]
rs1847963	0.82[ASN][1000 genomes]
rs1847967	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1847969	0.95[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.85[EUR][1000 genomes]
rs1857889	0.82[ASN][1000 genomes]
rs1911077	0.84[EUR][1000 genomes]
rs2048022	0.84[EUR][1000 genomes]
rs2083922	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2174584	0.84[EUR][1000 genomes]
rs2197322	0.95[CHB][hapmap]
rs28523416	0.84[EUR][1000 genomes]
rs28565871	0.86[EUR][1000 genomes]
rs28633781	0.82[ASN][1000 genomes]
rs28788633	0.84[EUR][1000 genomes]
rs35257138	0.84[EUR][1000 genomes]
rs36039803	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4293790	0.86[JPT][hapmap]
rs4414959	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4699283	0.87[EUR][1000 genomes]
rs4699285	0.85[EUR][1000 genomes]
rs4699287	0.83[EUR][1000 genomes]
rs4699483	0.89[ASN][1000 genomes]
rs4699485	0.93[ASN][1000 genomes]
rs5017329	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55847611	0.85[ASN][1000 genomes]
rs6532596	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6532597	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6532600	0.86[EUR][1000 genomes]
rs6815558	0.86[EUR][1000 genomes]
rs6826156	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6826817	0.88[ASN][1000 genomes]
rs6830120	0.84[EUR][1000 genomes]
rs6832934	0.84[EUR][1000 genomes]
rs6834542	0.91[ASN][1000 genomes]
rs6835808	0.81[ASN][1000 genomes]
rs6837318	0.84[CEU][hapmap]
rs72880179	0.83[ASN][1000 genomes]
rs72880182	0.83[ASN][1000 genomes]
rs7653937	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs766061	0.82[ASN][1000 genomes]
rs7665151	0.87[ASN][1000 genomes]
rs7671563	0.87[ASN][1000 genomes]
rs7671604	0.82[ASN][1000 genomes]
rs7673756	0.84[EUR][1000 genomes]
rs7676317	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7676764	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7686174	0.83[EUR][1000 genomes]
rs9307168	0.87[EUR][1000 genomes]
rs931841	0.84[EUR][1000 genomes]
rs9884259	0.96[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.85[EUR][1000 genomes]
rs9884940	0.84[EUR][1000 genomes]
rs9998383	0.85[CEU][hapmap];0.80[YRI][hapmap]
rs9999006	0.84[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830013	chr4:97033125-97204291	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1003868	chr4:97068155-97222544	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	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	chr4:97091600-97093000	Active TSS	K562	blood

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