Variant report

Variant	rs1241207
Chromosome Location	chr1:103337356-103337357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1020918	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1031820	0.88[AFR][1000 genomes]
rs1031821	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10782911	0.80[ASN][1000 genomes]
rs10874662	0.82[ASN][1000 genomes]
rs11164628	0.82[ASN][1000 genomes]
rs11164629	0.82[ASN][1000 genomes]
rs11164630	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs11164632	0.82[ASN][1000 genomes]
rs12023984	0.82[ASN][1000 genomes]
rs1241164	0.83[CEU][hapmap]
rs1241166	0.83[CEU][hapmap]
rs1241171	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1241179	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241181	0.81[CEU][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes]
rs1241182	0.81[CEU][hapmap]
rs1241183	0.81[CEU][hapmap];0.81[YRI][hapmap]
rs1241186	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241187	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1241194	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241196	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1241198	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241199	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241200	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1241201	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1241202	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1241205	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1241206	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1241208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1241209	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1261690	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1263061	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1270748	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1271798	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12722976	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12731405	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1318756	0.85[ASN][1000 genomes]
rs1463037	0.81[CEU][hapmap];0.80[YRI][hapmap]
rs1463038	0.83[CEU][hapmap];0.86[YRI][hapmap]
rs1463039	0.81[CEU][hapmap];0.89[YRI][hapmap]
rs1463048	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs1621055	0.81[CEU][hapmap];0.85[YRI][hapmap]
rs1622838	0.81[CEU][hapmap];0.85[YRI][hapmap]
rs1676491	0.86[AFR][1000 genomes]
rs1676493	0.81[CEU][hapmap];0.89[YRI][hapmap]
rs1676494	0.81[CEU][hapmap];0.89[YRI][hapmap]
rs1676495	0.81[YRI][hapmap]
rs1676497	0.83[CEU][hapmap]
rs1676498	0.81[CEU][hapmap];0.86[YRI][hapmap]
rs1676499	0.81[CEU][hapmap];0.85[YRI][hapmap]
rs1676500	0.83[CEU][hapmap];0.85[YRI][hapmap]
rs1676501	0.90[CEU][hapmap];0.82[YRI][hapmap]
rs1676502	0.82[YRI][hapmap]
rs1676507	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1676508	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1676510	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1763342	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1763343	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1763344	0.81[YRI][hapmap]
rs1763345	0.83[CEU][hapmap];0.86[YRI][hapmap]
rs1763346	0.83[CEU][hapmap];0.86[YRI][hapmap]
rs1763348	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1763349	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1763359	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1841841	0.82[ASN][1000 genomes]
rs1932331	0.82[ASN][1000 genomes]
rs2077569	0.82[ASN][1000 genomes]
rs2169608	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs2169609	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs2169610	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2229783	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs2615999	0.83[CEU][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs2616002	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2783566	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2783570	0.81[CEU][hapmap]
rs4907983	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4907985	0.86[ASN][1000 genomes]
rs4908270	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61157885	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs644019	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs68109992	0.86[AFR][1000 genomes]
rs899019	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs899020	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs945326	0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs969272	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830882	chr1:103192683-103355802	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv546928	chr1:103331349-103371652	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	nsv871829	chr1:103336601-103367095	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	nsv870600	chr1:103336601-103548497	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103334000-103349800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:103335400-103350000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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