Variant report

Variant	rs72726283
Chromosome Location	chr14:65370992-65370993
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11621450	0.85[EUR][1000 genomes]
rs11621527	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs11622077	0.87[EUR][1000 genomes]
rs11623705	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs11624878	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11625722	0.89[EUR][1000 genomes]
rs11626557	0.86[EUR][1000 genomes]
rs11629410	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17752452	0.85[EUR][1000 genomes]
rs17767942	0.89[EUR][1000 genomes]
rs17767960	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17880303	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17880939	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs17882875	0.85[EUR][1000 genomes]
rs17883358	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2277502	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4899156	0.82[EUR][1000 genomes]
rs4902331	0.89[EUR][1000 genomes]
rs4902347	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4902348	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4902349	0.85[EUR][1000 genomes]
rs4902350	0.82[EUR][1000 genomes]
rs4902351	0.85[EUR][1000 genomes]
rs60796816	0.89[EUR][1000 genomes]
rs7145282	0.83[EUR][1000 genomes]
rs72726275	0.87[EUR][1000 genomes]
rs72726294	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs72726300	0.89[EUR][1000 genomes]
rs72726301	0.89[EUR][1000 genomes]
rs72728209	0.85[EUR][1000 genomes]
rs72728213	0.86[EUR][1000 genomes]
rs72728215	0.87[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	esv3693169	chr14:65344400-65381068	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1311	chr14:65352722-65379802	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs72726283	CHURC1	cis	Heart Left Ventricle	GTEx
rs72726283	CHURC1	cis	lung	GTEx
rs72726283	CHURC1	cis	Skin Sun Exposed Lower leg	GTEx
rs72726283	CHURC1	cis	Thyroid	GTEx
rs72726283	CHURC1	cis	Artery Tibial	GTEx
rs72726283	CHURC1	cis	Muscle Skeletal	GTEx
rs72726283	CHURC1	cis	Whole Blood	GTEx

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

No data

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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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