Variant report

Variant	rs1606802
Chromosome Location	chr2:123821997-123821998
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10178398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1154994	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1154995	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1154996	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1154997	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1160010	0.88[EUR][1000 genomes]
rs1160011	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1160012	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12466984	0.94[ASN][1000 genomes]
rs12476143	0.89[ASN][1000 genomes]
rs12478792	0.94[ASN][1000 genomes]
rs12478793	0.94[ASN][1000 genomes]
rs12620936	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12996298	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13005367	0.80[EUR][1000 genomes]
rs13031371	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1395931	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1507667	0.83[EUR][1000 genomes]
rs17381599	0.89[ASN][1000 genomes]
rs17466105	0.89[ASN][1000 genomes]
rs188493	0.88[EUR][1000 genomes]
rs2063800	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2244129	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2248895	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2419071	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2458994	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2661001	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2661032	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2661035	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2661036	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2661041	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2661043	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2661044	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2661045	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2673182	0.90[EUR][1000 genomes]
rs2673185	0.89[EUR][1000 genomes]
rs2673187	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2673188	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2673189	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2673194	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2673196	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2900804	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs299536	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs299539	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs299540	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs299542	0.90[EUR][1000 genomes]
rs299544	0.85[CEU][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.91[JPT][hapmap];0.89[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs299545	0.90[EUR][1000 genomes]
rs299546	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs299548	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs299549	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs299550	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs299551	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs299553	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs299560	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs299561	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs299562	0.85[EUR][1000 genomes]
rs36131743	0.85[EUR][1000 genomes]
rs4848824	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6726973	0.94[ASN][1000 genomes]
rs6731851	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6734712	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6747893	0.89[EUR][1000 genomes]
rs6754344	0.89[ASN][1000 genomes]
rs6755603	0.94[ASN][1000 genomes]
rs6755929	0.94[ASN][1000 genomes]
rs6761730	0.89[ASN][1000 genomes]
rs7608420	0.94[ASN][1000 genomes]
rs7608426	0.94[ASN][1000 genomes]
rs7608772	0.94[ASN][1000 genomes]
rs7609057	0.89[ASN][1000 genomes]
rs957759	0.94[ASN][1000 genomes]
rs9636359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][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	nsv492280	chr2:123447662-123973577	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2760647	chr2:123678437-124619697	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1010200	chr2:123816326-123887210	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr2:123820200-123822000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:123821000-123822800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:123821400-123822200	Enhancers	Brain Germinal Matrix	brain

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