Variant report

Variant	rs12467604
Chromosome Location	chr2:182139108-182139109
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10175109	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10180754	0.90[AFR][1000 genomes]
rs10187534	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10197733	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10199252	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10200577	0.87[AFR][1000 genomes]
rs10206405	0.84[CEU][hapmap]
rs1023761	0.92[AFR][1000 genomes]
rs10497577	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10930963	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10930965	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10930966	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12617083	0.83[ASN][1000 genomes]
rs12622227	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12623524	0.86[ASN][1000 genomes]
rs12693273	0.92[AFR][1000 genomes]
rs12693274	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12992819	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13384115	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13387919	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13390496	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13390501	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13390598	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13393596	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13393709	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13400585	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13400592	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13400891	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13403977	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13413108	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13416416	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13419105	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13426182	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1371615	0.85[CEU][hapmap]
rs1371617	0.92[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1440045	0.93[AFR][1000 genomes]
rs17456058	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17456106	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17456148	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2077783	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2119148	0.82[ASN][1000 genomes]
rs2368200	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4255928	0.88[ASN][1000 genomes]
rs57063898	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57334172	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61235737	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61358146	0.84[ASN][1000 genomes]
rs62180207	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62180228	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62180237	0.84[ASN][1000 genomes]
rs62180238	0.82[ASN][1000 genomes]
rs62180239	0.82[ASN][1000 genomes]
rs6717513	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6717754	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6728366	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6729353	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6743422	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6743583	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6744081	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6757550	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs720453	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7564749	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7564976	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7602997	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9288064	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9288065	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs972605	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1002647	chr2:182078521-182392273	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536064	chr2:182078521-182392273	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182117800-182140200	Weak transcription	Dnd41	blood
2	chr2:182117800-182140600	Weak transcription	Fetal Thymus	thymus
3	chr2:182128400-182139800	Weak transcription	Primary T cells from cord blood	blood
4	chr2:182128400-182139800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr2:182135200-182139800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr2:182135400-182139800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:182137000-182139800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr2:182137000-182140600	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr2:182137200-182139800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr2:182137800-182140600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr2:182138400-182142200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:182138600-182139800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr2:182138600-182145200	Weak transcription	HSMMtube	muscle
14	chr2:182138800-182139800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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