Variant report

Variant	rs62166564
Chromosome Location	chr2:78200703-78200704
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1527177	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1527184	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609078	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17014854	0.86[ASN][1000 genomes]
rs17014856	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17597326	0.80[EUR][1000 genomes]
rs17657108	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59236450	0.80[EUR][1000 genomes]
rs62163507	0.87[EUR][1000 genomes]
rs62164367	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164369	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164371	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164372	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164382	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164383	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164384	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164385	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62164701	0.80[EUR][1000 genomes]
rs62164703	0.80[EUR][1000 genomes]
rs62164705	0.83[EUR][1000 genomes]
rs62164706	0.80[EUR][1000 genomes]
rs62164731	0.81[EUR][1000 genomes]
rs62166561	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62166562	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62166563	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62167312	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62167317	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62167318	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72817242	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7565330	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917204	chr2:78047538-78602013	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3329151	chr2:78071300-78271485	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1003166	chr2:78091352-78211828	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1001461	chr2:78091352-78673948	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv2757811	chr2:78126389-78711032	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2759068	chr2:78126389-78711032	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1003010	chr2:78145703-78219800	Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1010580	chr2:78171642-78206296	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1000527	chr2:78176225-78468796	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv3449162	chr2:78181346-78221434	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	esv3404781	chr2:78186346-78220877	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	esv3447123	chr2:78186346-78239095	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv517285	chr2:78199268-78204327	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv524980	chr2:78199268-78218826	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	esv2756933	chr2:78199735-78640246	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78199200-78201800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:78200000-78200800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr2:78200200-78201200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr2:78200400-78201400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr2:78200600-78201000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:78200600-78201800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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