Variant report

Variant	rs10256309
Chromosome Location	chr7:69048942-69048943
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10229578	0.90[AMR][1000 genomes]
rs10233869	0.90[AMR][1000 genomes]
rs10236103	0.85[ASN][1000 genomes]
rs10238307	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10241446	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10245493	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10248237	0.90[AMR][1000 genomes]
rs10255613	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10256311	0.95[ASN][1000 genomes]
rs10256512	0.90[AMR][1000 genomes]
rs10256943	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10257587	0.90[AMR][1000 genomes]
rs10261380	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10261510	0.86[ASN][1000 genomes]
rs10268221	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10268457	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10276664	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10280018	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10281575	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10281579	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11762049	0.90[AMR][1000 genomes]
rs11773581	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12334231	0.85[ASN][1000 genomes]
rs12334234	0.90[ASN][1000 genomes]
rs17140693	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17140755	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17140759	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17140783	0.90[AMR][1000 genomes]
rs17140817	0.90[AMR][1000 genomes]
rs2068718	0.90[AMR][1000 genomes]
rs28493290	1.00[AMR][1000 genomes]
rs28524600	0.95[ASN][1000 genomes]
rs3735260	0.90[ASN][1000 genomes]
rs55693719	0.95[ASN][1000 genomes]
rs55847506	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55901635	0.86[ASN][1000 genomes]
rs56800568	0.85[ASN][1000 genomes]
rs59342262	0.86[ASN][1000 genomes]
rs59517352	0.86[ASN][1000 genomes]
rs61692535	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61744589	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62454937	1.00[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs62454938	0.95[ASN][1000 genomes]
rs6950638	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6951770	0.85[ASN][1000 genomes]
rs6962237	0.84[AMR][1000 genomes]
rs6977472	0.85[ASN][1000 genomes]
rs717266	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73155227	0.95[ASN][1000 genomes]
rs73164795	0.90[AMR][1000 genomes]
rs73167506	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73170852	0.90[AMR][1000 genomes]
rs73170857	0.90[AMR][1000 genomes]
rs73170864	0.90[AMR][1000 genomes]
rs7357113	0.95[ASN][1000 genomes]
rs7777269	0.90[AMR][1000 genomes]
rs7787342	0.95[ASN][1000 genomes]
rs7787695	0.87[ASN][1000 genomes]
rs7810982	0.81[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	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	nsv428169	chr7:69021482-69196743	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv5783	chr7:69048608-69066760	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69048400-69051000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:69048800-69051400	Enhancers	Fetal Intestine Small	intestine
3	chr7:69048800-69052400	Enhancers	Fetal Intestine Large	intestine

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