Variant report

Variant	rs4858910
Chromosome Location	chr3:162432004-162432005
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:30)

rs_ID	r²[population]
rs11922500	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13083886	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1874510	0.92[AMR][1000 genomes]
rs1874512	0.92[AMR][1000 genomes]
rs2029925	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56242739	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6414407	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6441540	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6441541	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6441543	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6441545	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6764576	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6778765	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7427964	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7427978	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7433902	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7630042	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7634217	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7646046	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7652432	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9810012	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9813079	0.87[AMR][1000 genomes]
rs9815701	0.80[AMR][1000 genomes]
rs9831314	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9832503	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9859307	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9870314	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9878965	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9882410	0.92[AMR][1000 genomes]
rs9882755	0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006802	chr3:161921063-162599175	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv428424	chr3:162145988-163033943	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012160	chr3:162182166-162540478	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv592201	chr3:162188625-163142162	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470994	chr3:162217993-162945834	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1005142	chr3:162284967-162447818	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv877758	chr3:162287573-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv877759	chr3:162303276-162521339	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv877761	chr3:162346392-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv592208	chr3:162369863-162437102	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1005637	chr3:162379324-162635451	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv877762	chr3:162400620-162521339	Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv869804	chr3:162414099-162776884	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv829776	chr3:162422424-162577578	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	nsv1001282	chr3:162429561-162513137	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162430800-162436600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:162431200-162432600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr3:162431400-162432600	Weak transcription	Dnd41	blood
4	chr3:162431800-162432400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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