Variant report

Variant	rs6668963
Chromosome Location	chr1:76153140-76153141
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:76152720..76155791-chr1:76253617..76257786,3	K562	blood:

Variant related genes	Relation type
ENSG00000137955	Chromatin interaction
ENSG00000201487	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10782556	0.85[ASN][1000 genomes]
rs11161439	0.91[ASN][1000 genomes]
rs11161447	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11161465	0.87[ASN][1000 genomes]
rs11161600	0.83[ASN][1000 genomes]
rs11161602	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11161605	0.81[ASN][1000 genomes]
rs11164015	0.81[ASN][1000 genomes]
rs11164035	0.91[ASN][1000 genomes]
rs11164037	0.91[ASN][1000 genomes]
rs12021750	0.81[ASN][1000 genomes]
rs12022011	0.86[ASN][1000 genomes]
rs12024645	0.85[ASN][1000 genomes]
rs12027620	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12031600	0.84[ASN][1000 genomes]
rs12032051	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12033058	0.85[ASN][1000 genomes]
rs12033059	0.85[ASN][1000 genomes]
rs12034697	0.94[ASN][1000 genomes]
rs12044025	0.81[ASN][1000 genomes]
rs12045299	0.94[ASN][1000 genomes]
rs12045363	0.85[ASN][1000 genomes]
rs12049212	0.84[ASN][1000 genomes]
rs12404553	0.94[ASN][1000 genomes]
rs12407107	0.85[ASN][1000 genomes]
rs1251077	0.81[ASN][1000 genomes]
rs12563737	0.86[ASN][1000 genomes]
rs12564772	0.85[ASN][1000 genomes]
rs12724860	0.81[ASN][1000 genomes]
rs12728962	0.83[ASN][1000 genomes]
rs12732722	0.88[ASN][1000 genomes]
rs12736447	0.88[ASN][1000 genomes]
rs12744608	0.83[ASN][1000 genomes]
rs12745456	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12747967	0.91[ASN][1000 genomes]
rs12755811	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12756349	0.83[ASN][1000 genomes]
rs12757213	0.82[ASN][1000 genomes]
rs1391518	0.91[ASN][1000 genomes]
rs1391520	0.91[ASN][1000 genomes]
rs1535740	0.94[ASN][1000 genomes]
rs1591120	0.94[ASN][1000 genomes]
rs17097634	0.85[ASN][1000 genomes]
rs1826978	0.82[ASN][1000 genomes]
rs2131558	0.85[ASN][1000 genomes]
rs34486572	0.85[ASN][1000 genomes]
rs35290302	0.84[ASN][1000 genomes]
rs35837767	0.91[ASN][1000 genomes]
rs3737574	0.84[ASN][1000 genomes]
rs5745314	0.86[ASN][1000 genomes]
rs5745334	0.85[ASN][1000 genomes]
rs5745353	0.81[ASN][1000 genomes]
rs5745426	0.84[ASN][1000 genomes]
rs5745429	0.84[ASN][1000 genomes]
rs58552356	0.84[ASN][1000 genomes]
rs6665431	0.88[ASN][1000 genomes]
rs6676182	0.86[ASN][1000 genomes]
rs6695055	0.88[ASN][1000 genomes]
rs67108483	0.91[ASN][1000 genomes]
rs7417486	0.94[ASN][1000 genomes]
rs7525919	0.85[ASN][1000 genomes]
rs7548695	0.85[ASN][1000 genomes]
rs7548991	0.82[ASN][1000 genomes]
rs814897	0.82[ASN][1000 genomes]
rs815301	0.93[ASN][1000 genomes]
rs815305	0.89[ASN][1000 genomes]
rs9660848	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2757737	chr1:75986904-76187748	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv2758943	chr1:75986904-76187748	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv427675	chr1:76070382-76187748	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2756846	chr1:76083408-76156986	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv870520	chr1:76088392-76206490	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv830281	chr1:76095292-76251053	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv945914	chr1:76109781-76172388	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

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
chromosomal regions: chr1:12345-34567

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