Variant report

Variant	rs1870441
Chromosome Location	chr3:48398459-48398460
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:48392357..48396827-chr3:48398052..48401684,5	MCF-7	breast:
2	chr3:48341311..48343466-chr3:48397822..48400484,2	MCF-7	breast:
3	chr3:48387745..48390068-chr3:48395716..48398672,2	MCF-7	breast:
4	chr3:48348380..48351660-chr3:48396274..48399024,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000172113	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11130161	1.00[YRI][hapmap]
rs12630599	0.90[EUR][1000 genomes]
rs13062576	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1380260	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1459243	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1459244	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1459245	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1459247	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs17080119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34138269	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34537842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34857497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35703936	0.92[AFR][1000 genomes]
rs3731532	1.00[YRI][hapmap]
rs3731539	1.00[YRI][hapmap]
rs3731547	1.00[YRI][hapmap]
rs4858813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4858814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4858818	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs6793732	0.80[AFR][1000 genomes]
rs876597	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs9852211	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs986739	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs986740	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs986741	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs986742	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

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	nsv834683	chr3:48301504-48493261	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv834684	chr3:48385699-48589323	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48397000-48398800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:48397400-48398600	Weak transcription	Pancreas	Pancrea
3	chr3:48397400-48399600	Enhancers	HepG2	liver

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