Variant report

Variant	rs4668407
Chromosome Location	chr2:172534884-172534885
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10206062	0.82[EUR][1000 genomes]
rs10803863	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs11678984	0.83[EUR][1000 genomes]
rs12053003	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs12185567	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12692970	0.81[EUR][1000 genomes]
rs13419987	0.80[EUR][1000 genomes]
rs13429113	0.82[EUR][1000 genomes]
rs1554166	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2357061	0.82[EUR][1000 genomes]
rs2674484	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs312916	0.81[EUR][1000 genomes]
rs312918	0.80[EUR][1000 genomes]
rs312924	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs312925	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs34542126	0.82[EUR][1000 genomes]
rs35549875	0.81[EUR][1000 genomes]
rs3795999	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4668412	0.80[EUR][1000 genomes]
rs6433311	0.81[EUR][1000 genomes]
rs6709156	0.80[EUR][1000 genomes]
rs6721680	0.84[EUR][1000 genomes]
rs6722757	0.80[EUR][1000 genomes]
rs6757773	0.81[EUR][1000 genomes]
rs71013062	0.81[EUR][1000 genomes]
rs7597387	0.80[EUR][1000 genomes]
rs973889	0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997638	chr2:172442205-172560406	Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs4668407	AC068039.4	cis	Stomach	GTEx
rs4668407	AC068039.4	cis	Skin Sun Exposed Lower leg	GTEx
rs4668407	AC068039.4	cis	lung	GTEx
rs4668407	AC068039.4	cis	Muscle Skeletal	GTEx
rs4668407	AC068039.4	cis	Esophagus Muscularis	GTEx
rs4668407	AC068039.4	cis	Thyroid	GTEx
rs4668407	AC068039.4	cis	Adipose Subcutaneous	GTEx
rs4668407	AC068039.4	cis	Esophagus Mucosa	GTEx
rs4668407	AC068039.4	cis	Whole Blood	GTEx
rs4668407	AC068039.4	cis	Nerve Tibial	GTEx
rs4668407	SLC25A12	Cis_1M	lymphoblastoid	RTeQTL

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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