Variant report

Variant	rs34956502
Chromosome Location	chr12:10446646-10446647
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	chr12:10445022..10447315-chr12:10448355..10450390,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10743881	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10845099	0.81[EUR][1000 genomes]
rs10845104	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11053701	0.86[ASN][1000 genomes]
rs11053722	0.97[EUR][1000 genomes]
rs11612335	0.87[ASN][1000 genomes]
rs12302171	0.83[ASN][1000 genomes]
rs12303774	0.86[ASN][1000 genomes]
rs12304713	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12311695	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12315681	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12315815	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12813575	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12814085	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12817905	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12818742	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12821332	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12824930	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12828163	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12828540	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12829898	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12831232	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12832221	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12832489	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17206564	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2537765	0.84[ASN][1000 genomes]
rs2537793	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537805	0.90[ASN][1000 genomes]
rs2617128	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2617135	0.97[EUR][1000 genomes]
rs2617137	0.97[EUR][1000 genomes]
rs2927558	0.97[EUR][1000 genomes]
rs34282122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34790670	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34859528	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35510688	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs35518026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35868193	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4346056	0.85[ASN][1000 genomes]
rs4365134	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4764369	0.98[EUR][1000 genomes]
rs56272210	0.98[ASN][1000 genomes]
rs58700703	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7136409	0.80[EUR][1000 genomes]
rs71450031	0.85[ASN][1000 genomes]
rs71450032	0.85[ASN][1000 genomes]
rs71450033	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71450034	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs765792	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7958472	0.97[EUR][1000 genomes]
rs7963011	0.86[ASN][1000 genomes]
rs7969664	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832328	chr12:10398071-10620443	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10445200-10446800	Enhancers	Thymus	Thymus
2	chr12:10445200-10447000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr12:10445200-10447000	Enhancers	GM12878-XiMat	blood
4	chr12:10445200-10447200	Enhancers	Fetal Thymus	thymus
5	chr12:10445200-10447600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr12:10445400-10447000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr12:10445400-10447800	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr12:10445800-10447400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:10446000-10446800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
10	chr12:10446000-10446800	Enhancers	Dnd41	blood
11	chr12:10446000-10447000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:10446000-10447000	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr12:10446000-10447400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr12:10446200-10446800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr12:10446200-10446800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr12:10446400-10446800	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr12:10446600-10447800	Enhancers	Primary T cells from cord blood	blood

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