Variant report

Variant	rs10261510
Chromosome Location	chr7:68978117-68978118
allele	A/G
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:41)

rs_ID	r²[population]
rs10236103	0.82[ASN][1000 genomes]
rs10238307	0.82[ASN][1000 genomes]
rs10241446	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10245493	0.91[ASN][1000 genomes]
rs10255613	0.91[ASN][1000 genomes]
rs10256309	0.86[ASN][1000 genomes]
rs10256311	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10256943	0.82[ASN][1000 genomes]
rs10261380	0.82[ASN][1000 genomes]
rs10268221	0.86[ASN][1000 genomes]
rs10268457	0.86[ASN][1000 genomes]
rs10276664	0.89[ASN][1000 genomes]
rs10280018	0.89[ASN][1000 genomes]
rs10281575	0.86[ASN][1000 genomes]
rs10281579	0.86[ASN][1000 genomes]
rs11773581	0.86[ASN][1000 genomes]
rs12334231	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12334234	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17140693	0.91[ASN][1000 genomes]
rs28524600	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3735260	0.86[ASN][1000 genomes]
rs55693719	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55847506	0.91[ASN][1000 genomes]
rs55901635	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56800568	0.82[ASN][1000 genomes]
rs59342262	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59517352	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61692535	0.91[ASN][1000 genomes]
rs61744589	0.89[ASN][1000 genomes]
rs62454894	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62454937	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62454938	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6950638	0.82[ASN][1000 genomes]
rs6951770	0.82[ASN][1000 genomes]
rs6977472	0.82[ASN][1000 genomes]
rs717266	0.82[ASN][1000 genomes]
rs73155227	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73167506	0.82[ASN][1000 genomes]
rs7357113	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7787342	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7787695	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023885	chr7:68894896-69158290	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538915	chr7:68894896-69158290	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv916011	chr7:68942155-69330800	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv5782	chr7:68946883-68991904	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr7:68975400-68983000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:68976600-68980400	Weak transcription	Fetal Heart	heart

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