Variant report

Variant	rs11979353
Chromosome Location	chr7:12197179-12197180
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:12197065..12199564-chr7:12248019..12250882,2	K562	blood:

Variant related genes	Relation type
ENSG00000106460	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1020007	0.83[EUR][1000 genomes]
rs10235641	0.87[EUR][1000 genomes]
rs10250890	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10260421	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10950387	0.87[EUR][1000 genomes]
rs10950388	0.87[EUR][1000 genomes]
rs11977383	0.87[EUR][1000 genomes]
rs11977384	0.87[EUR][1000 genomes]
rs11979354	0.88[EUR][1000 genomes]
rs11980922	0.87[EUR][1000 genomes]
rs12531743	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12534492	0.87[EUR][1000 genomes]
rs12536685	0.87[EUR][1000 genomes]
rs12536705	0.87[EUR][1000 genomes]
rs12537306	0.87[EUR][1000 genomes]
rs12537337	0.86[EUR][1000 genomes]
rs12539665	0.87[EUR][1000 genomes]
rs12699312	0.87[EUR][1000 genomes]
rs12699313	0.87[EUR][1000 genomes]
rs12699314	0.87[EUR][1000 genomes]
rs13226876	0.84[EUR][1000 genomes]
rs13228832	0.80[EUR][1000 genomes]
rs13230297	0.87[EUR][1000 genomes]
rs13232977	0.87[EUR][1000 genomes]
rs13232992	0.87[EUR][1000 genomes]
rs13233005	0.87[EUR][1000 genomes]
rs13233228	0.87[EUR][1000 genomes]
rs13233611	0.87[EUR][1000 genomes]
rs13241051	0.87[EUR][1000 genomes]
rs13241891	0.87[EUR][1000 genomes]
rs13241969	0.87[EUR][1000 genomes]
rs13243169	0.87[EUR][1000 genomes]
rs13244303	0.86[EUR][1000 genomes]
rs13245840	0.87[EUR][1000 genomes]
rs13245891	0.87[EUR][1000 genomes]
rs13306984	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13307377	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1347436	0.87[EUR][1000 genomes]
rs34201361	0.80[EUR][1000 genomes]
rs36104470	0.80[EUR][1000 genomes]
rs59509870	0.82[ASN][1000 genomes]
rs6947317	0.82[ASN][1000 genomes]
rs6948974	0.87[EUR][1000 genomes]
rs6952453	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6967233	0.87[EUR][1000 genomes]
rs6978380	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6978570	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6978632	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6978650	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs71533421	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs71533422	0.87[EUR][1000 genomes]
rs7780991	0.86[EUR][1000 genomes]
rs7783565	0.87[EUR][1000 genomes]
rs7783576	0.87[EUR][1000 genomes]
rs7783947	0.87[EUR][1000 genomes]
rs7784236	0.89[EUR][1000 genomes]
rs7788029	0.87[EUR][1000 genomes]
rs7788225	0.87[EUR][1000 genomes]
rs7788563	0.89[EUR][1000 genomes]
rs7788670	0.82[EUR][1000 genomes]
rs7795567	0.81[EUR][1000 genomes]
rs7802974	0.89[EUR][1000 genomes]
rs7804819	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv1021710	chr7:12164993-12251790	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
6	nsv887627	chr7:12178793-12227892	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv887628	chr7:12186502-12227892	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12194800-12198400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:12197000-12197400	Weak transcription	A549	lung

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