Variant report

Variant	rs7016694
Chromosome Location	chr8:66899723-66899724
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16932426	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16932433	0.91[ASN][1000 genomes]
rs17307227	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2357571	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4380923	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4495411	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4549750	0.86[ASN][1000 genomes]
rs58902647	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62506635	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62506642	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62506643	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62506644	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62506646	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62507392	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6985796	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7006334	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7011399	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7823449	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7836993	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7846530	0.99[EUR][1000 genomes];0.95[ASN][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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66893800-66901800	Weak transcription	Spleen	Spleen
2	chr8:66894800-66904000	Weak transcription	Primary T cells from cord blood	blood
3	chr8:66894800-66904400	Weak transcription	Thymus	Thymus
4	chr8:66895000-66904400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr8:66895200-66900200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr8:66898200-66900600	Weak transcription	Primary B cells from peripheral blood	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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