Variant report

Variant	rs298041
Chromosome Location	chr5:58928272-58928273
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10805516	0.93[ASN][1000 genomes]
rs159196	0.83[ASN][1000 genomes]
rs159197	0.83[ASN][1000 genomes]
rs177077	0.85[ASN][1000 genomes]
rs177078	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs190936	0.93[ASN][1000 genomes]
rs294492	0.83[ASN][1000 genomes]
rs294495	0.85[ASN][1000 genomes]
rs294496	0.85[ASN][1000 genomes]
rs294497	0.85[ASN][1000 genomes]
rs294498	0.83[ASN][1000 genomes]
rs294499	0.84[ASN][1000 genomes]
rs294500	0.84[ASN][1000 genomes]
rs294501	0.83[ASN][1000 genomes]
rs294502	0.82[ASN][1000 genomes]
rs295944	0.87[ASN][1000 genomes]
rs295948	0.84[ASN][1000 genomes]
rs295950	0.89[ASN][1000 genomes]
rs295951	0.89[ASN][1000 genomes]
rs295953	0.89[ASN][1000 genomes]
rs295954	0.89[ASN][1000 genomes]
rs295955	0.89[ASN][1000 genomes]
rs295956	0.89[ASN][1000 genomes]
rs295957	0.89[ASN][1000 genomes]
rs295958	0.90[ASN][1000 genomes]
rs295960	0.90[ASN][1000 genomes]
rs295962	0.93[ASN][1000 genomes]
rs295963	0.93[ASN][1000 genomes]
rs295964	0.93[ASN][1000 genomes]
rs295965	0.93[ASN][1000 genomes]
rs295966	0.93[ASN][1000 genomes]
rs295967	0.93[ASN][1000 genomes]
rs295968	0.93[ASN][1000 genomes]
rs295969	0.93[ASN][1000 genomes]
rs295970	0.93[ASN][1000 genomes]
rs295971	0.93[ASN][1000 genomes]
rs295972	0.93[ASN][1000 genomes]
rs295973	0.92[ASN][1000 genomes]
rs295974	0.93[ASN][1000 genomes]
rs295975	0.93[ASN][1000 genomes]
rs295978	0.87[ASN][1000 genomes]
rs295980	0.87[ASN][1000 genomes]
rs298014	0.92[ASN][1000 genomes]
rs298016	0.93[ASN][1000 genomes]
rs298017	0.93[ASN][1000 genomes]
rs298018	0.81[ASN][1000 genomes]
rs298025	0.83[ASN][1000 genomes]
rs298027	0.83[ASN][1000 genomes]
rs298028	0.83[ASN][1000 genomes]
rs298029	0.83[ASN][1000 genomes]
rs298030	0.85[ASN][1000 genomes]
rs298032	0.89[ASN][1000 genomes]
rs298033	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs298034	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs298036	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs298037	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs298038	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs298039	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs298040	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs298043	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs298044	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298045	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298046	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs298047	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298051	0.96[ASN][1000 genomes]
rs298052	0.96[ASN][1000 genomes]
rs298053	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031631	chr5:58783629-59015470	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv881708	chr5:58869051-59093198	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1018015	chr5:58889470-59532667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv537766	chr5:58889470-59532667	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv598256	chr5:58893286-58939840	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv598257	chr5:58905769-58946639	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv427720	chr5:58913581-59086987	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58911400-58929600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:58923600-58957200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:58923800-58945000	Weak transcription	Aorta	Aorta
4	chr5:58925800-58933600	Weak transcription	A549	lung
5	chr5:58926000-58928600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:58926800-58934000	Weak transcription	Hela-S3	cervix
7	chr5:58927000-58939800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:58927800-58928400	Strong transcription	Fetal Intestine Small	intestine
9	chr5:58927800-58928400	ZNF genes & repeats	Fetal Stomach	stomach
10	chr5:58928200-58928400	Enhancers	Gastric	stomach

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