Variant report

Variant	rs1503430
Chromosome Location	chr3:87942715-87942716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1156395	0.84[AFR][1000 genomes]
rs11926472	0.86[EUR][1000 genomes]
rs12492995	0.86[EUR][1000 genomes]
rs13324246	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1354324	0.89[ASN][1000 genomes]
rs1393915	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1465648	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1503425	0.89[AFR][1000 genomes]
rs1503426	0.89[AFR][1000 genomes]
rs1503428	0.93[AFR][1000 genomes]
rs1503429	0.87[ASN][1000 genomes]
rs1604701	0.89[AFR][1000 genomes]
rs17025121	0.87[ASN][1000 genomes]
rs17025198	0.87[EUR][1000 genomes]
rs17025201	0.85[EUR][1000 genomes]
rs1864617	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1875715	0.84[ASN][1000 genomes]
rs1946570	0.87[ASN][1000 genomes]
rs2062811	0.89[AFR][1000 genomes]
rs2062812	0.86[ASN][1000 genomes]
rs2116145	0.86[EUR][1000 genomes]
rs2915288	0.85[AFR][1000 genomes]
rs2919267	0.85[AFR][1000 genomes]
rs2919272	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2919282	0.81[ASN][1000 genomes]
rs2932274	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2932277	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2932284	0.81[ASN][1000 genomes]
rs2932301	0.90[AFR][1000 genomes]
rs2938261	0.81[ASN][1000 genomes]
rs2938264	0.84[ASN][1000 genomes]
rs2938265	0.89[AFR][1000 genomes]
rs2938268	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2938270	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2938271	0.81[ASN][1000 genomes]
rs2938272	0.81[ASN][1000 genomes]
rs34979865	0.86[ASN][1000 genomes]
rs6551260	0.86[EUR][1000 genomes]
rs6764864	0.87[ASN][1000 genomes]
rs73847730	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7619960	0.83[AFR][1000 genomes]
rs9310058	0.86[EUR][1000 genomes]
rs9836185	0.85[EUR][1000 genomes]
rs9850490	0.85[EUR][1000 genomes]
rs9869636	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs989563	0.89[AFR][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	nsv1009981	chr3:87821573-88003956	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv536634	chr3:87821573-88003956	Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv460757	chr3:87863280-87949733	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv590919	chr3:87863280-87949733	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv834758	chr3:87867363-88014975	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv2760794	chr3:87932310-87953742	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1001572	chr3:87942288-87983962	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:87938800-87946800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:87941400-87944400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:87942600-87947400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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