Variant report

Variant	rs10011791
Chromosome Location	chr4:99863716-99863717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10007957	0.93[ASN][1000 genomes]
rs10008093	0.93[ASN][1000 genomes]
rs10010610	0.89[ASN][1000 genomes]
rs10019506	0.95[ASN][1000 genomes]
rs10020687	0.92[ASN][1000 genomes]
rs10022521	0.95[ASN][1000 genomes]
rs10032966	0.89[ASN][1000 genomes]
rs10212891	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1036946	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10433891	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10433976	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10461135	0.93[ASN][1000 genomes]
rs10470955	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10516437	0.89[ASN][1000 genomes]
rs11725932	0.89[ASN][1000 genomes]
rs11728783	0.89[ASN][1000 genomes]
rs11737130	0.88[ASN][1000 genomes]
rs11737186	0.88[ASN][1000 genomes]
rs1230147	0.96[ASN][1000 genomes]
rs1230149	0.98[ASN][1000 genomes]
rs1230150	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1230152	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1230189	0.88[ASN][1000 genomes]
rs17028238	0.93[ASN][1000 genomes]
rs17028241	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17028244	0.93[ASN][1000 genomes]
rs17028293	0.94[ASN][1000 genomes]
rs17550514	0.93[ASN][1000 genomes]
rs2602889	0.92[ASN][1000 genomes]
rs28367437	0.95[ASN][1000 genomes]
rs28376834	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28430857	0.90[ASN][1000 genomes]
rs28473608	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28499420	0.91[ASN][1000 genomes]
rs28529446	0.91[ASN][1000 genomes]
rs28575093	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28577966	0.90[ASN][1000 genomes]
rs28589528	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28613604	0.90[ASN][1000 genomes]
rs28622595	1.00[ASN][1000 genomes]
rs28633499	0.93[ASN][1000 genomes]
rs3133161	0.96[ASN][1000 genomes]
rs35447189	0.98[ASN][1000 genomes]
rs4699370	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60120090	0.93[ASN][1000 genomes]
rs60658326	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6532774	0.93[ASN][1000 genomes]
rs6815444	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6830125	0.91[ASN][1000 genomes]
rs6841295	0.90[ASN][1000 genomes]
rs6846266	0.90[ASN][1000 genomes]
rs6846475	0.89[ASN][1000 genomes]
rs72677504	0.93[ASN][1000 genomes]
rs72692622	0.91[ASN][1000 genomes]
rs7660937	0.92[ASN][1000 genomes]
rs7661487	0.94[ASN][1000 genomes]
rs7664964	0.90[ASN][1000 genomes]
rs7666015	0.99[ASN][1000 genomes]
rs7671306	0.91[ASN][1000 genomes]
rs7671453	0.91[ASN][1000 genomes]
rs7674319	0.90[ASN][1000 genomes]
rs7676504	0.91[ASN][1000 genomes]
rs7679685	1.00[ASN][1000 genomes]
rs7684964	0.91[ASN][1000 genomes]
rs7696573	0.90[ASN][1000 genomes]
rs7696584	0.90[ASN][1000 genomes]
rs7697071	0.90[ASN][1000 genomes]
rs9332467	0.90[ASN][1000 genomes]
rs994636	0.91[ASN][1000 genomes]
rs9995478	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9996959	0.94[ASN][1000 genomes]
rs9999702	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv879654	chr4:99748988-99877402	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 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	chr4:99860200-99866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:99861000-99867200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:99861200-99866000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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