Variant report

Variant	rs59165380
Chromosome Location	chr13:80141083-80141084
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10492579	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10507899	0.89[EUR][1000 genomes]
rs1335373	0.82[EUR][1000 genomes]
rs1414157	0.89[EUR][1000 genomes]
rs17071499	0.82[EUR][1000 genomes]
rs17071532	0.89[EUR][1000 genomes]
rs17071549	0.85[EUR][1000 genomes]
rs17071558	0.82[EUR][1000 genomes]
rs17071566	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17071574	0.89[EUR][1000 genomes]
rs17071585	0.89[EUR][1000 genomes]
rs17071627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17071632	0.82[EUR][1000 genomes]
rs41288268	0.82[EUR][1000 genomes]
rs56711390	0.89[EUR][1000 genomes]
rs57032852	0.89[EUR][1000 genomes]
rs57929179	0.85[EUR][1000 genomes]
rs58406632	0.89[EUR][1000 genomes]
rs59381369	0.82[EUR][1000 genomes]
rs59783325	0.89[EUR][1000 genomes]
rs60126328	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61318325	0.85[EUR][1000 genomes]
rs61676417	0.89[EUR][1000 genomes]
rs6563117	0.89[EUR][1000 genomes]
rs7317409	0.82[EUR][1000 genomes]
rs7317511	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7318854	0.82[EUR][1000 genomes]
rs7327148	0.89[EUR][1000 genomes]
rs7338043	0.89[EUR][1000 genomes]
rs73548951	0.82[EUR][1000 genomes]
rs73548955	0.82[EUR][1000 genomes]
rs73551558	0.82[EUR][1000 genomes]
rs73551595	0.89[EUR][1000 genomes]
rs73551596	0.89[EUR][1000 genomes]
rs73551597	0.89[EUR][1000 genomes]
rs73551601	0.89[EUR][1000 genomes]
rs73551602	0.89[EUR][1000 genomes]
rs73553403	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73553418	0.85[EUR][1000 genomes]
rs73553424	0.89[EUR][1000 genomes]
rs73553431	0.89[EUR][1000 genomes]
rs73553447	0.89[EUR][1000 genomes]
rs73553448	0.85[EUR][1000 genomes]
rs73553473	0.89[EUR][1000 genomes]
rs73553481	0.85[EUR][1000 genomes]
rs73553499	0.82[EUR][1000 genomes]
rs73555411	0.82[EUR][1000 genomes]
rs73555415	0.82[EUR][1000 genomes]
rs7491258	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7981574	0.89[EUR][1000 genomes]
rs7984159	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7984598	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7985697	0.82[EUR][1000 genomes]
rs7990190	0.89[EUR][1000 genomes]
rs7990464	0.89[EUR][1000 genomes]
rs7998452	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8000870	0.82[EUR][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	nsv916983	chr13:80065879-80249702	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1041994	chr13:80123596-80247708	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 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	chr13:80135600-80147200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:80140600-80155800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:80141000-80141200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin

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