Variant report

Variant	rs398555
Chromosome Location	chr3:83426801-83426802
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	chr3:83425432..83427800-chr3:83443567..83446268,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1020614	0.90[EUR][1000 genomes]
rs1020615	0.90[EUR][1000 genomes]
rs1020616	0.88[EUR][1000 genomes]
rs12714565	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12714566	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13061386	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452167	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452179	0.89[EUR][1000 genomes]
rs1452180	0.90[EUR][1000 genomes]
rs1551232	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs164273	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2198281	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28859986	0.89[EUR][1000 genomes]
rs28893195	0.85[EUR][1000 genomes]
rs67529822	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67764414	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs700013	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7648751	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9811230	0.97[EUR][1000 genomes]
rs9811656	0.82[EUR][1000 genomes]
rs9812521	0.89[EUR][1000 genomes]
rs9842201	0.82[EUR][1000 genomes]
rs9865924	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9867218	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9869072	0.82[EUR][1000 genomes]
rs9878614	0.89[EUR][1000 genomes]
rs9882209	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008268	chr3:83057096-83476080	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv536608	chr3:83057096-83476080	Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv998408	chr3:83057096-83549271	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv536609	chr3:83057096-83549271	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3324557	chr3:83153978-83450434	Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv877071	chr3:83324183-83536528	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv3432916	chr3:83390311-83432689	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv1006081	chr3:83421626-84262106	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr3:83425800-83427200	Enhancers	Dnd41	blood

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