Variant report

Variant	rs252049
Chromosome Location	chr5:52567976-52567977
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs153129	0.94[AMR][1000 genomes]
rs251519	0.89[AMR][1000 genomes]
rs251520	0.89[AMR][1000 genomes]
rs251522	0.86[AMR][1000 genomes]
rs251525	0.87[AMR][1000 genomes]
rs251528	0.95[AMR][1000 genomes]
rs251531	0.81[AMR][1000 genomes]
rs252034	0.84[AMR][1000 genomes]
rs252035	0.84[AMR][1000 genomes]
rs252038	0.83[AMR][1000 genomes]
rs252040	0.81[AMR][1000 genomes]
rs252041	0.80[AMR][1000 genomes]
rs252042	0.84[AMR][1000 genomes]
rs252050	0.95[AMR][1000 genomes]
rs252051	0.95[AMR][1000 genomes]
rs252053	0.83[AMR][1000 genomes]
rs252054	0.87[AMR][1000 genomes]
rs27967	0.87[AMR][1000 genomes]
rs370753	0.84[AMR][1000 genomes]
rs37776	0.81[AMR][1000 genomes]
rs37777	0.83[AMR][1000 genomes]
rs37778	0.83[AMR][1000 genomes]
rs37807	0.89[AMR][1000 genomes]
rs38055	0.94[AMR][1000 genomes]
rs38056	0.95[AMR][1000 genomes]
rs38058	0.95[AMR][1000 genomes]
rs384866	0.84[AMR][1000 genomes]
rs40230	0.87[AMR][1000 genomes]
rs40232	0.95[AMR][1000 genomes]
rs408393	0.84[AMR][1000 genomes]
rs435548	0.89[AMR][1000 genomes]
rs454737	0.94[AMR][1000 genomes]
rs565253	0.89[AMR][1000 genomes]
rs574790	0.83[AMR][1000 genomes]
rs584593	0.83[AMR][1000 genomes]
rs626726	0.84[AMR][1000 genomes]
rs629725	0.84[AMR][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	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv830297	chr5:52492494-52707758	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv522454	chr5:52492677-52571758	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:52563800-52575200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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