Variant report

Variant	rs1869023
Chromosome Location	chr11:25946371-25946372
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANO3-2	chr11:25945687-25946841	NONHSAT018453

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10501027	0.85[EUR][1000 genomes]
rs10834839	0.82[ASN][1000 genomes]
rs10834840	0.82[ASN][1000 genomes]
rs10834841	0.82[ASN][1000 genomes]
rs10834852	0.92[ASN][1000 genomes]
rs10834853	0.92[ASN][1000 genomes]
rs11029008	0.81[ASN][1000 genomes]
rs11029009	0.81[ASN][1000 genomes]
rs11029011	0.82[ASN][1000 genomes]
rs11029031	0.84[ASN][1000 genomes]
rs11029032	0.84[ASN][1000 genomes]
rs11029044	0.81[ASN][1000 genomes]
rs11529818	0.84[ASN][1000 genomes]
rs12223680	0.81[ASN][1000 genomes]
rs12796585	0.88[EUR][1000 genomes]
rs12803523	0.90[EUR][1000 genomes]
rs1441511	0.85[EUR][1000 genomes]
rs16914888	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16914903	0.90[ASN][1000 genomes]
rs16914910	0.90[EUR][1000 genomes]
rs182757	0.81[ASN][1000 genomes]
rs2349600	0.86[ASN][1000 genomes]
rs67141149	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs7104765	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7106427	0.86[EUR][1000 genomes]
rs72875022	0.86[EUR][1000 genomes]
rs72875027	0.86[EUR][1000 genomes]
rs72875031	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv832091	chr11:25823826-26009887	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv469948	chr11:25859783-26026233	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1041778	chr11:25898574-26098141	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv897140	chr11:25905509-25991194	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv467775	chr11:25916225-25957544	Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv553896	chr11:25916225-25957544	Enhancers Weak transcription Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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