Variant report

Variant	rs13126499
Chromosome Location	chr4:175675011-175675012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11133054	0.83[EUR][1000 genomes]
rs11133055	0.83[EUR][1000 genomes]
rs11945237	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13110718	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1385838	0.83[EUR][1000 genomes]
rs1385839	0.83[EUR][1000 genomes]
rs36082225	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4695961	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4695962	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6553817	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6553823	0.83[EUR][1000 genomes]
rs6553825	0.83[EUR][1000 genomes]
rs6553827	0.83[EUR][1000 genomes]
rs6553828	0.83[EUR][1000 genomes]
rs6825415	0.83[EUR][1000 genomes]
rs6825619	0.83[EUR][1000 genomes]
rs6826181	0.83[EUR][1000 genomes]
rs7687424	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1018390	chr4:175475505-175969742	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1034301	chr4:175656538-176055348	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv537364	chr4:175656538-176055348	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1030235	chr4:175663839-175969742	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv537365	chr4:175663839-175969742	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr4:175674600-175675200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr4:175674800-175675400	Enhancers	Fetal Brain Male	brain

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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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