Variant report

Variant	rs11065436
Chromosome Location	chr12:121556151-121556152
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:121548947..121551862-chr12:121555011..121556681,2	MCF-7	breast:
2	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
3	chr12:121531941..121534103-chr12:121555507..121557731,2	K562	blood:
4	chr12:121554481..121556246-chr12:121646405..121649275,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000135124	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10849843	0.96[ASN][1000 genomes]
rs10849845	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10849846	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10849848	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10849849	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10849850	0.93[ASN][1000 genomes]
rs10849851	0.91[ASN][1000 genomes]
rs11065428	0.93[ASN][1000 genomes]
rs11065433	0.98[ASN][1000 genomes]
rs11065435	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11065437	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11065440	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11065441	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11065443	0.99[ASN][1000 genomes]
rs11065445	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11065453	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11065458	0.92[ASN][1000 genomes]
rs208292	0.92[ASN][1000 genomes]
rs2393800	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3861798	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3891262	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3900976	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4077055	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4559762	0.98[ASN][1000 genomes]
rs58717055	0.99[ASN][1000 genomes]
rs6489794	0.92[ASN][1000 genomes]
rs684201	0.96[ASN][1000 genomes]
rs7298521	0.98[ASN][1000 genomes]
rs7302184	0.95[ASN][1000 genomes]
rs7310821	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7313004	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7314706	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7954687	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv899559	chr12:121324727-121592689	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv899560	chr12:121371233-121560581	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv899562	chr12:121376416-121565870	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv2758318	chr12:121415845-121584813	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv2759917	chr12:121415845-121584813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv832531	chr12:121440495-121604232	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
9	nsv430537	chr12:121487632-121579955	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	nsv899563	chr12:121543011-121600529	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv1050519	chr12:121552964-121756420	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121552400-121560800	Weak transcription	K562	blood
2	chr12:121552600-121557800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:121555400-121557200	Weak transcription	Spleen	Spleen
4	chr12:121555400-121565800	Weak transcription	Gastric	stomach
5	chr12:121555800-121561600	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links