Variant report

Variant	rs10863573
Chromosome Location	chr1:221117700-221117701
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10495159	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10779417	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10779418	0.90[EUR][1000 genomes]
rs11118632	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12022930	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.82[YRI][hapmap];0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12140805	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1335927	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1335929	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1414519	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1414520	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2484703	0.96[CEU][hapmap];0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs2484704	0.91[EUR][1000 genomes]
rs2484706	0.92[EUR][1000 genomes]
rs2784276	0.90[EUR][1000 genomes]
rs2784279	0.92[EUR][1000 genomes]
rs2784280	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2784281	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2807832	0.90[EUR][1000 genomes]
rs2807875	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2807876	0.92[EUR][1000 genomes]
rs2807877	0.92[EUR][1000 genomes]
rs2807881	0.96[CEU][hapmap];0.83[CHB][hapmap];0.91[EUR][1000 genomes]
rs2992647	0.88[EUR][1000 genomes]
rs2992649	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2992650	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3013553	0.89[EUR][1000 genomes]
rs3013554	0.88[EUR][1000 genomes]
rs3013556	0.86[EUR][1000 genomes]
rs3013558	0.86[EUR][1000 genomes]
rs6678632	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	esv3321206	chr1:221113643-221118806	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3321208	chr1:221113684-221118789	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3321205	chr1:221113711-221118750	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3321209	chr1:221113785-221118699	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221116800-221117800	Enhancers	Colon Smooth Muscle	Colon

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