Variant report

Variant	rs10497018
Chromosome Location	chr2:148457312-148457313
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10170800	0.80[EUR][1000 genomes]
rs10181608	0.80[EUR][1000 genomes]
rs10183294	0.80[EUR][1000 genomes]
rs10469566	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1113958	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464481	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464921	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12464985	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12465277	0.80[EUR][1000 genomes]
rs12467064	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12467429	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12468864	0.81[EUR][1000 genomes]
rs12474024	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691767	0.81[ASN][1000 genomes]
rs12988552	0.80[EUR][1000 genomes]
rs13004499	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13014274	0.80[EUR][1000 genomes]
rs13026223	0.81[EUR][1000 genomes]
rs13033070	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1406447	0.84[ASN][1000 genomes]
rs1424944	0.81[CEU][hapmap]
rs1528837	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16827722	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1919440	0.80[EUR][1000 genomes]
rs1919441	0.80[EUR][1000 genomes]
rs35826590	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35905220	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4662292	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4662293	0.81[EUR][1000 genomes]
rs4662548	0.84[ASN][1000 genomes]
rs6706259	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6721628	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7564409	0.80[EUR][1000 genomes]
rs7568718	0.81[EUR][1000 genomes]
rs7581116	0.81[ASN][1000 genomes]
rs7590862	0.80[EUR][1000 genomes]
rs7595433	0.81[ASN][1000 genomes]
rs7605932	0.81[EUR][1000 genomes]
rs9653190	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875275	chr2:148166428-148711242	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv916286	chr2:148438001-148977722	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148457200-148457400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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