Variant report

Variant	rs2992325
Chromosome Location	chr10:26711491-26711492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11595895	0.88[EUR][1000 genomes]
rs12770943	0.81[EUR][1000 genomes]
rs12783726	0.96[EUR][1000 genomes]
rs12783831	0.94[EUR][1000 genomes]
rs1335540	0.92[EUR][1000 genomes]
rs1335551	0.96[EUR][1000 genomes]
rs1335552	0.96[EUR][1000 genomes]
rs1889686	0.81[EUR][1000 genomes]
rs1889692	0.95[EUR][1000 genomes]
rs1889693	0.95[EUR][1000 genomes]
rs2184571	0.95[EUR][1000 genomes]
rs2992261	0.82[EUR][1000 genomes]
rs2992262	0.82[EUR][1000 genomes]
rs2992263	0.82[EUR][1000 genomes]
rs2992332	0.96[EUR][1000 genomes]
rs2992333	0.87[EUR][1000 genomes]
rs2992334	0.89[EUR][1000 genomes]
rs2992335	0.92[EUR][1000 genomes]
rs3006802	0.81[EUR][1000 genomes]
rs3006807	0.96[EUR][1000 genomes]
rs3006808	0.96[EUR][1000 genomes]
rs3006810	0.96[EUR][1000 genomes]
rs3006811	0.96[EUR][1000 genomes]
rs3006813	0.96[EUR][1000 genomes]
rs3006815	0.95[EUR][1000 genomes]
rs3006816	0.96[EUR][1000 genomes]
rs3006818	0.96[EUR][1000 genomes]
rs3006819	0.94[EUR][1000 genomes]
rs3006821	0.96[EUR][1000 genomes]
rs3006835	0.81[EUR][1000 genomes]
rs35055608	0.95[EUR][1000 genomes]
rs36120850	0.95[EUR][1000 genomes]
rs4749125	0.91[EUR][1000 genomes]
rs4749126	0.92[EUR][1000 genomes]
rs59819668	0.81[EUR][1000 genomes]
rs7098710	0.89[EUR][1000 genomes]
rs7901056	0.95[EUR][1000 genomes]
rs9284109	0.95[EUR][1000 genomes]
rs9299819	0.95[EUR][1000 genomes]
rs9299820	0.96[EUR][1000 genomes]
rs9299821	0.96[EUR][1000 genomes]
rs945294	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv1043832	chr10:26669040-26809400	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2992325	APBB1IP	cis	Thyroid	GTEx
rs2992325	APBB1IP	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26711400-26713400	Enhancers	Primary monocytes fromperipheralblood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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