Variant report

Variant	rs73268211
Chromosome Location	chr12:10708646-10708647
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs59582425	0.86[AMR][1000 genomes]
rs7309605	0.86[AMR][1000 genomes]
rs73252010	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73252011	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73252012	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73252013	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73252057	0.86[AMR][1000 genomes]
rs73266202	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268205	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268207	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268209	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268213	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268214	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268219	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268220	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060420	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7957198	0.86[AMR][1000 genomes]
rs7959470	0.93[AMR][1000 genomes]
rs7959753	0.93[AMR][1000 genomes]
rs7961522	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs7974801	0.93[AMR][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	nsv898766	chr12:10537269-10722585	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv557459	chr12:10560591-10729821	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv898772	chr12:10622047-10722585	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv557479	chr12:10644663-10729821	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv898773	chr12:10660850-10722585	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv898774	chr12:10666025-10722585	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv898775	chr12:10668694-10735786	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1039120	chr12:10675930-10755446	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv832329	chr12:10677094-10845946	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10707400-10709800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
2	chr12:10707800-10710000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:10707800-10710200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:10707800-10711200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:10707800-10713200	Enhancers	Dnd41	blood
6	chr12:10708200-10709200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:10708200-10709600	Active TSS	Primary T cells from cord blood	blood
8	chr12:10708200-10709600	Weak transcription	GM12878-XiMat	blood
9	chr12:10708200-10709800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:10708200-10709800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:10708200-10709800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr12:10708200-10709800	Weak transcription	Fetal Thymus	thymus
13	chr12:10708200-10709800	Weak transcription	Thymus	Thymus

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