Variant report

Variant	rs10073130
Chromosome Location	chr5:128306267-128306268
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	chr5:128289643..128291319-chr5:128306001..128308500,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11953704	0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs154590	0.92[AMR][1000 genomes]
rs185411	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2526254	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2577420	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs257896	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257897	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257898	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257899	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257900	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257901	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257903	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257904	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs257905	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs257908	0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs257999	0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs258000	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs258002	0.99[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs258004	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4629641	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4836424	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs976944	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882839	chr5:128205828-128390167	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv882840	chr5:128205828-128428962	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830485	chr5:128298622-128480492	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
4	nsv882841	chr5:128301971-128400356	Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv882842	chr5:128301971-128552706	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:128303000-128308800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:128303000-128309000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:128303200-128312600	Weak transcription	Fetal Heart	heart
4	chr5:128303400-128319400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr5:128304200-128311000	Weak transcription	Fetal Stomach	stomach

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