Variant report

Variant	rs12429858
Chromosome Location	chr13:38486031-38486032
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	chr13:38485175..38486789-chr13:38490324..38493116,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12429104	1.00[YRI][hapmap]
rs1337594	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1337595	0.83[EUR][1000 genomes]
rs1337605	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1337607	0.86[EUR][1000 genomes]
rs1415599	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1415628	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1556781	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2210979	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2485286	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2485291	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2485298	0.88[CHB][hapmap]
rs2485483	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34544559	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35140422	0.83[AFR][1000 genomes]
rs4943548	0.86[EUR][1000 genomes]
rs4943551	0.86[EUR][1000 genomes]
rs6563572	0.84[EUR][1000 genomes]
rs6563573	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6563574	0.84[EUR][1000 genomes]
rs71423167	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7322764	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7327323	0.94[ASN][1000 genomes]
rs7336052	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7992543	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7994671	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7994826	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs817729	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9315526	0.86[EUR][1000 genomes]
rs945858	0.86[EUR][1000 genomes]
rs945859	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9548093	0.89[ASN][1000 genomes]
rs9548104	0.86[EUR][1000 genomes]
rs9548107	0.86[EUR][1000 genomes]
rs9548108	0.84[EUR][1000 genomes]
rs9548109	0.86[EUR][1000 genomes]
rs9566279	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9576402	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9576405	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9576406	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9576424	0.83[AFR][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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv899996	chr13:38459224-38577056	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv899997	chr13:38480878-38518459	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv899998	chr13:38480878-38582178	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38484200-38488200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:38484200-38494200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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