Variant report

Variant	rs12364661
Chromosome Location	chr11:45484320-45484321
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:45475301..45477081-chr11:45482793..45484529,2	K562	blood:

Extended variants
information (count: 146 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs10160472	1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]
rs10160502	1.00[CEU][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]
rs10160694	0.90[EUR][1000 genomes]
rs10160834	0.90[EUR][1000 genomes]
rs10501315	0.98[EUR][1000 genomes]
rs10838454	0.90[EUR][1000 genomes]
rs10838455	0.90[EUR][1000 genomes]
rs10838479	0.98[EUR][1000 genomes]
rs11038403	0.84[EUR][1000 genomes]
rs11038404	0.88[EUR][1000 genomes]
rs11038405	0.88[EUR][1000 genomes]
rs11038406	0.90[EUR][1000 genomes]
rs11038409	0.88[EUR][1000 genomes]
rs11038411	0.90[EUR][1000 genomes]
rs11038417	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs11038420	0.90[EUR][1000 genomes]
rs11038423	0.90[EUR][1000 genomes]
rs11038424	0.90[EUR][1000 genomes]
rs11038426	0.90[EUR][1000 genomes]
rs11038427	0.90[EUR][1000 genomes]
rs11038429	0.93[EUR][1000 genomes]
rs11038431	0.96[EUR][1000 genomes]
rs11038432	0.96[EUR][1000 genomes]
rs11038433	0.96[EUR][1000 genomes]
rs11038434	0.98[EUR][1000 genomes]
rs11038435	0.98[EUR][1000 genomes]
rs11038437	0.98[EUR][1000 genomes]
rs11038442	0.98[EUR][1000 genomes]
rs11038443	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs11038444	0.98[EUR][1000 genomes]
rs11038450	1.00[EUR][1000 genomes]
rs11038451	1.00[EUR][1000 genomes]
rs11038455	1.00[EUR][1000 genomes]
rs11038456	1.00[EUR][1000 genomes]
rs11038457	1.00[EUR][1000 genomes]
rs11038458	1.00[EUR][1000 genomes]
rs11038459	0.98[EUR][1000 genomes]
rs11038461	0.96[EUR][1000 genomes]
rs11038462	1.00[EUR][1000 genomes]
rs11038465	1.00[EUR][1000 genomes]
rs11038466	1.00[EUR][1000 genomes]
rs11038467	1.00[EUR][1000 genomes]
rs11038469	1.00[EUR][1000 genomes]
rs11038471	0.98[EUR][1000 genomes]
rs11038472	0.96[EUR][1000 genomes]
rs11038473	1.00[EUR][1000 genomes]
rs11038474	1.00[EUR][1000 genomes]
rs11038475	1.00[EUR][1000 genomes]
rs11038477	1.00[EUR][1000 genomes]
rs11038479	1.00[EUR][1000 genomes]
rs11038481	1.00[EUR][1000 genomes]
rs11038482	1.00[EUR][1000 genomes]
rs11038483	0.98[EUR][1000 genomes]
rs11038485	0.96[EUR][1000 genomes]
rs11038486	0.98[EUR][1000 genomes]
rs11038487	0.98[EUR][1000 genomes]
rs11038491	0.93[EUR][1000 genomes]
rs11038492	0.98[EUR][1000 genomes]
rs11038493	0.98[EUR][1000 genomes]
rs11038494	0.98[EUR][1000 genomes]
rs11038495	0.98[EUR][1000 genomes]
rs11038496	0.98[EUR][1000 genomes]
rs11038497	0.98[EUR][1000 genomes]
rs11038498	0.98[EUR][1000 genomes]
rs11038510	0.85[EUR][1000 genomes]
rs11038515	0.89[EUR][1000 genomes]
rs11038516	0.89[EUR][1000 genomes]
rs11038518	0.89[EUR][1000 genomes]
rs11038520	0.89[EUR][1000 genomes]
rs11038522	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs11038525	0.87[CEU][hapmap]
rs11038528	0.87[CEU][hapmap]
rs11038543	0.85[CEU][hapmap]
rs11038549	0.87[CEU][hapmap]
rs11038550	0.87[CEU][hapmap]
rs11038551	0.87[CEU][hapmap]
rs11038552	1.00[CEU][hapmap]
rs1107209	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11599949	0.88[EUR][1000 genomes]
rs11599993	0.88[EUR][1000 genomes]
rs11601006	0.90[EUR][1000 genomes]
rs11601410	0.90[EUR][1000 genomes]
rs11604510	0.90[EUR][1000 genomes]
rs12278000	0.90[EUR][1000 genomes]
rs12360696	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12361372	1.00[EUR][1000 genomes]
rs12363740	0.96[EUR][1000 genomes]
rs12364278	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12365374	0.90[EUR][1000 genomes]
rs12365430	1.00[EUR][1000 genomes]
rs12365455	0.90[EUR][1000 genomes]
rs12365467	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs12365982	0.98[EUR][1000 genomes]
rs12366014	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1488668	0.98[EUR][1000 genomes]
rs1488669	0.98[EUR][1000 genomes]
rs1488670	0.98[EUR][1000 genomes]
rs16938268	0.86[AFR][1000 genomes]
rs17723819	1.00[EUR][1000 genomes]
rs17724032	0.98[EUR][1000 genomes]
rs17724086	0.98[EUR][1000 genomes]
rs17724240	0.87[CEU][hapmap];1.00[GIH][hapmap]
rs17785901	0.98[EUR][1000 genomes]
rs17786039	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs17786178	0.86[CEU][hapmap]
rs1844150	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2044877	0.91[EUR][1000 genomes]
rs72893316	0.91[EUR][1000 genomes]
rs72893332	0.87[EUR][1000 genomes]
rs72893337	0.87[EUR][1000 genomes]
rs72893356	0.89[EUR][1000 genomes]
rs72897413	0.90[EUR][1000 genomes]
rs72897414	0.90[EUR][1000 genomes]
rs72897422	0.90[EUR][1000 genomes]
rs72897428	0.90[EUR][1000 genomes]
rs72897458	0.90[EUR][1000 genomes]
rs72897475	0.96[EUR][1000 genomes]
rs72899452	0.87[EUR][1000 genomes]
rs72899480	0.98[EUR][1000 genomes]
rs72899488	1.00[EUR][1000 genomes]
rs72901403	1.00[EUR][1000 genomes]
rs72901422	1.00[EUR][1000 genomes]
rs72901426	1.00[EUR][1000 genomes]
rs72901447	1.00[EUR][1000 genomes]
rs72901450	1.00[EUR][1000 genomes]
rs72901459	1.00[EUR][1000 genomes]
rs72901500	1.00[EUR][1000 genomes]
rs72903035	1.00[EUR][1000 genomes]
rs72903086	1.00[EUR][1000 genomes]
rs72903094	1.00[EUR][1000 genomes]
rs72905021	0.98[EUR][1000 genomes]
rs72905025	0.98[EUR][1000 genomes]
rs72905092	0.98[EUR][1000 genomes]
rs72905093	0.98[EUR][1000 genomes]
rs72906922	0.98[EUR][1000 genomes]
rs72906947	0.94[EUR][1000 genomes]
rs971897	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1045831	chr11:45419113-45580407	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049520	chr11:45430802-45494235	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv541026	chr11:45430802-45494235	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	nsv1050657	chr11:45455431-45484320	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv1035430	chr11:45455431-45487231	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	nsv1035254	chr11:45457183-45487231	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv1053919	chr11:45457920-45506491	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv541027	chr11:45457920-45506491	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45478600-45485000	Weak transcription	Pancreas	Pancrea
2	chr11:45483800-45484800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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