Variant report

Variant	rs10825380
Chromosome Location	chr10:56469974-56469975
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10825379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004454	1.00[ASN][1000 genomes]
rs11004456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004458	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004459	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11004461	1.00[ASN][1000 genomes]
rs11004462	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17592217	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1832185	0.97[EUR][1000 genomes]
rs1932601	0.97[EUR][1000 genomes]
rs4935118	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935119	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935120	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4935545	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58286973	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67776107	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7073425	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72794533	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72794592	0.81[EUR][1000 genomes]
rs7900549	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050405	chr10:56224676-56800009	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv540635	chr10:56224676-56800009	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv933410	chr10:56319433-56713977	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1043144	chr10:56332903-56680265	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv550970	chr10:56361499-56764751	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
6	esv2758221	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2759754	chr10:56408027-56566137	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv895447	chr10:56428277-56587755	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2757387	chr10:56436508-56473754	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1809742	chr10:56441343-56474113	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1829325	chr10:56442061-56514009	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv1818753	chr10:56445570-56472693	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv1792554	chr10:56445730-56470990	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1815358	chr10:56445730-56470990	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv1826784	chr10:56445730-56470990	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv1811548	chr10:56446810-56472693	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv1850921	chr10:56447391-56470758	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv1843743	chr10:56448129-56470990	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv2829926	chr10:56448886-56474910	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv1835020	chr10:56448886-56478284	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv550975	chr10:56448886-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv1838385	chr10:56452937-56472860	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv1043472	chr10:56452937-56479771	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv895448	chr10:56456576-56526747	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv1039277	chr10:56456775-56485231	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv550980	chr10:56461036-56473373	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv550981	chr10:56461036-56474910	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
28	esv1838177	chr10:56462471-56478751	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
29	esv1831037	chr10:56462471-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
30	nsv526545	chr10:56462471-56554972	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
31	esv1825751	chr10:56467657-56494207	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
32	esv1832833	chr10:56467874-56494301	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
33	esv3417658	chr10:56468546-56470894	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
34	esv1826456	chr10:56468563-56493670	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
35	esv14427	chr10:56469623-56503557	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56466400-56471000	Enhancers	Fetal Lung	lung
2	chr10:56469200-56470600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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