Variant report

Variant	rs35121635
Chromosome Location	chr3:111023019-111023020
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:19)

rs_ID	r²[population]
rs12495444	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1489024	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1489040	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1590132	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1881675	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1881676	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1906703	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2130075	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2130076	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2634545	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2958067	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2971349	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4682249	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs923393	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9814916	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9819786	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9821540	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9869246	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9879486	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv829675	chr3:110885605-111101858	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv877339	chr3:110889974-111070554	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111017800-111023800	Enhancers	Dnd41	blood
2	chr3:111019400-111029400	Weak transcription	Thymus	Thymus
3	chr3:111019800-111023600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr3:111022000-111023800	Enhancers	Fetal Thymus	thymus
5	chr3:111023000-111023200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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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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