Variant report

Variant	rs12226823
Chromosome Location	chr11:36760982-36760983
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	chr11:36760152..36763496-chr11:36764810..36767505,3	K562	blood:

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10501162	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836594	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10836595	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836596	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836597	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836598	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836599	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836600	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836601	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836603	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836604	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10836605	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033765	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11033766	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033768	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033769	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033770	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11033774	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033775	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11033776	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11033779	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11033781	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11033782	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11033799	0.85[EUR][1000 genomes]
rs11033804	0.88[EUR][1000 genomes]
rs12099215	0.88[EUR][1000 genomes]
rs12221669	0.83[AMR][1000 genomes]
rs12223146	0.90[EUR][1000 genomes]
rs12223727	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12225581	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12225583	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12271535	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12271541	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12276665	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12276715	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12279194	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12280907	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12281077	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12284660	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12294055	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12294160	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12294236	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1401289	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1401290	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1401291	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1518745	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1589177	0.83[EUR][1000 genomes]
rs16929349	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1967545	0.88[EUR][1000 genomes]
rs1996536	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1996537	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2139137	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2139138	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2176594	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2422361	0.83[EUR][1000 genomes]
rs2901722	0.83[EUR][1000 genomes]
rs34465358	0.80[EUR][1000 genomes]
rs35299175	0.88[EUR][1000 genomes]
rs4332497	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4332498	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4582952	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4755456	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4755457	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4755459	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756336	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756337	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4756338	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756339	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756340	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756341	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4756342	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55877156	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56111224	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61078470	0.83[AMR][1000 genomes]
rs61877683	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61877684	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61877685	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61877686	0.84[EUR][1000 genomes]
rs61877687	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72947155	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7929934	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7933480	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs908786	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv467792	chr11:36624187-36898373	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv554005	chr11:36624187-36898373	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv467793	chr11:36632515-37171833	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv554006	chr11:36632515-37171833	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1047073	chr11:36711638-36812910	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1041508	chr11:36711638-36815367	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1043391	chr11:36711638-36817144	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv554007	chr11:36711834-36825618	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv11137	chr11:36730247-36788022	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	esv2761663	chr11:36730335-36786817	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36759600-36761000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:36759600-36761400	Enhancers	Thymus	Thymus
3	chr11:36759600-36761600	Enhancers	Fetal Thymus	thymus
4	chr11:36759600-36761600	Enhancers	Dnd41	blood
5	chr11:36759800-36761000	Enhancers	Primary hematopoietic stem cells	blood
6	chr11:36759800-36761200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr11:36759800-36761400	Enhancers	GM12878-XiMat	blood
8	chr11:36760000-36761000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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