Variant report

Variant	rs11182724
Chromosome Location	chr12:45265397-45265398
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10506259	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10880694	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10880698	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10880699	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10880727	1.00[AMR][1000 genomes]
rs10880728	1.00[AMR][1000 genomes]
rs10880729	1.00[AMR][1000 genomes]
rs11182700	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11182704	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182709	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11182712	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182713	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182714	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182717	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182722	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182723	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182725	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182726	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182728	0.94[ASN][1000 genomes]
rs11182729	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182730	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182770	1.00[AMR][1000 genomes]
rs11182771	1.00[AMR][1000 genomes]
rs11182772	1.00[AMR][1000 genomes]
rs11182785	1.00[AMR][1000 genomes]
rs11182789	1.00[AMR][1000 genomes]
rs11182790	1.00[AMR][1000 genomes]
rs11182791	1.00[AMR][1000 genomes]
rs11182792	1.00[AMR][1000 genomes]
rs11182793	1.00[AMR][1000 genomes]
rs11182796	0.87[AMR][1000 genomes]
rs11182798	0.87[AMR][1000 genomes]
rs12227311	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12227622	0.89[AMR][1000 genomes]
rs12228073	1.00[AMR][1000 genomes]
rs12228476	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12580287	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12581903	1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12582602	1.00[AMR][1000 genomes]
rs12829945	0.89[AMR][1000 genomes]
rs17095196	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17095198	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2658949	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2703049	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2703052	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2703056	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2703057	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2710418	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57726055	1.00[AMR][1000 genomes]
rs59646766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61438749	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71459276	0.97[ASN][1000 genomes]
rs7300104	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832394	chr12:45077573-45269305	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
2	nsv1036926	chr12:45131884-45273648	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv541484	chr12:45131884-45273648	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45257000-45266800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr12:45258600-45265600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:45258600-45267800	Weak transcription	Brain Germinal Matrix	brain
4	chr12:45259600-45266000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:45260000-45268000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:45261200-45265400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:45262000-45267800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr12:45263000-45269000	Active TSS	Fetal Brain Female	brain
9	chr12:45263400-45266400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:45263600-45265400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr12:45264600-45265400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:45264800-45265600	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr12:45264800-45266600	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr12:45264800-45266800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr12:45264800-45271200	Active TSS	Fetal Brain Male	brain
16	chr12:45265000-45265600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr12:45265200-45265600	Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr12:45265200-45266400	Enhancers	Primary T cells from cord blood	blood
19	chr12:45265200-45266400	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr12:45265200-45266600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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