Variant report

Variant	rs73986687
Chromosome Location	chr2:209897294-209897295
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH2R-2	chr2:209896369-209898538	l_2022_chr2:209894596-209898538_76bGuttman_hES

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs55836807	0.83[AMR][1000 genomes]
rs55984377	0.83[AMR][1000 genomes]
rs56784517	1.00[AMR][1000 genomes]
rs57099283	1.00[AMR][1000 genomes]
rs57820610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58494981	1.00[AMR][1000 genomes]
rs60615254	0.83[AMR][1000 genomes]
rs60788347	1.00[AMR][1000 genomes]
rs73983904	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73986658	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73986659	1.00[AMR][1000 genomes]
rs73986660	0.83[AMR][1000 genomes]
rs73986670	1.00[AMR][1000 genomes]
rs73986671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73986672	1.00[AMR][1000 genomes]
rs73986674	1.00[AMR][1000 genomes]
rs73986676	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73986677	1.00[AMR][1000 genomes]
rs73986689	0.83[AMR][1000 genomes]
rs73986695	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012184	chr2:209755847-210049331	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv536131	chr2:209755847-210049331	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3487576	chr2:209768379-209947296	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3487577	chr2:209768379-209947296	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1009924	chr2:209805661-210042572	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv875760	chr2:209817526-209929978	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1002578	chr2:209836205-210026339	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv536132	chr2:209836205-210026339	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv3371175	chr2:209886495-209902409	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
10	nsv516581	chr2:209894054-209899788	Inactive region	lncRNA	n/a	inside rSNPs	n/a

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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