Variant report

Variant	rs1167616
Chromosome Location	chr12:26047430-26047431
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10771244	0.83[AMR][1000 genomes]
rs10771246	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10771247	0.87[AFR][1000 genomes]
rs1167618	0.82[AFR][1000 genomes]
rs1167621	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1167622	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1177525	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1179567	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1183807	0.87[AFR][1000 genomes]
rs1797970	0.82[AMR][1000 genomes]
rs2634170	0.84[AFR][1000 genomes]
rs2634171	0.81[AMR][1000 genomes]
rs2643928	0.84[AFR][1000 genomes]
rs7307605	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs829821	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs829834	0.85[AMR][1000 genomes]
rs862621	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs865504	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs995795	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1035319	chr12:26020667-26097148	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26045000-26049800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:26045400-26049800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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Input of quick search could be:

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

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