Variant report

Variant	rs696501
Chromosome Location	chr3:22946675-22946676
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1671868	0.86[EUR][1000 genomes]
rs1671884	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1683043	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1683074	0.86[EUR][1000 genomes]
rs1708146	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs298416	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs33103	0.82[EUR][1000 genomes]
rs33104	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs33114	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3914284	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4858467	0.88[EUR][1000 genomes]
rs62252313	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs637382	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs696492	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs696502	0.96[EUR][1000 genomes]
rs696503	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs696504	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs696508	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs696509	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs698224	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs698228	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs698232	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs711698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs711699	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs711704	0.87[EUR][1000 genomes]
rs711707	0.89[EUR][1000 genomes]
rs711708	0.86[EUR][1000 genomes]
rs711709	0.86[EUR][1000 genomes]
rs822754	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs822756	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs822757	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs822758	0.86[EUR][1000 genomes]
rs822779	0.88[EUR][1000 genomes]
rs822781	0.88[EUR][1000 genomes]
rs822783	0.88[EUR][1000 genomes]
rs822784	0.81[EUR][1000 genomes]
rs822785	0.81[EUR][1000 genomes]
rs822786	0.88[EUR][1000 genomes]
rs822787	0.81[EUR][1000 genomes]
rs822788	0.88[EUR][1000 genomes]
rs822789	0.81[EUR][1000 genomes]
rs822791	0.85[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	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv16397	chr3:22941523-22946888	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22945800-22947000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:22946000-22947200	Enhancers	Fetal Lung	lung
3	chr3:22946400-22947000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:22946600-22946800	Enhancers	Fetal Stomach	stomach
5	chr3:22946600-22947000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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