Variant report

Variant	rs4867210
Chromosome Location	chr5:29852459-29852460
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFF	chr5:29852423-29853025	HepG2	liver:	n/a	chr5:29852593-29852611 chr5:29852599-29852613
2	MAFK	chr5:29852448-29852763	H1-hESC	embryonic stem cell:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606
3	MAFK	chr5:29852425-29853084	HepG2	liver:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606
4	MAFK	chr5:29852427-29852897	K562	blood:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606
5	MAFK	chr5:29852420-29853023	HepG2	liver:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606
6	MAFK	chr5:29852427-29852988	IMR90	lung:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606
7	MAFF	chr5:29852433-29852899	K562	blood:	n/a	chr5:29852593-29852611 chr5:29852599-29852613
8	MAFK	chr5:29852454-29853093	Hela-S3	cervix:	n/a	chr5:29852599-29852613 chr5:29852598-29852614 chr5:29852595-29852610 chr5:29852595-29852606 chr5:29852600-29852610 chr5:29852595-29852611 chr5:29852596-29852616 chr5:29852595-29852606

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:29852340..29854743-chr5:29859491..29862426,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000249744	TF binding region

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10055234	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10078174	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12153594	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12522268	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13172931	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1366309	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1428310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1428313	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1428319	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1428320	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1428322	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1428344	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1978607	1.00[JPT][hapmap];0.85[YRI][hapmap]
rs2052839	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2115186	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2914135	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2925527	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2972785	0.87[ASN][1000 genomes]
rs2972793	0.87[ASN][1000 genomes]
rs4315931	0.87[ASN][1000 genomes]
rs4352612	0.87[ASN][1000 genomes]
rs4416614	0.87[ASN][1000 genomes]
rs5025815	0.81[ASN][1000 genomes]
rs6450723	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450725	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7723603	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385368	chr5:29548608-29910057	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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