Variant report

Variant	rs2229569
Chromosome Location	chr1:169673838-169673839
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	WRNIP1	chr1:169673677-169673875	GM12878	blood:	n/a	n/a
2	IKZF1	chr1:169673827-169673937	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
SELL	TF binding region

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1051091	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1076637	0.91[EUR][1000 genomes]
rs1076638	0.91[EUR][1000 genomes]
rs10919228	0.90[EUR][1000 genomes]
rs12072966	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs12076368	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12079552	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12087033	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12131780	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1883228	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1883229	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1961877	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2205847	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2205849	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2420503	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs28469136	0.90[EUR][1000 genomes]
rs35289447	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3766129	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3917423	0.91[EUR][1000 genomes]
rs3917430	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3917435	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4427452	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4656698	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4987266	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4987298	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4987314	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4987328	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs5359	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58662634	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59807249	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6427212	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7513119	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs964555	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs964556	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs964557	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532586	chr1:169593222-169713184	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv872539	chr1:169658586-169674590	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1009313	chr1:169661299-169680173	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv872541	chr1:169672360-169695815	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169662400-169676000	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr1:169663200-169674000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:169664000-169674000	Genic enhancers	Fetal Thymus	thymus
4	chr1:169664000-169674200	Genic enhancers	Primary T cells fromperipheralblood	blood
5	chr1:169667600-169676800	Genic enhancers	Primary monocytes fromperipheralblood	blood
6	chr1:169668000-169677400	Transcr. at gene 5' and 3'	Primary T cells from cord blood	blood
7	chr1:169669600-169674400	Genic enhancers	Primary hematopoietic stem cells	blood
8	chr1:169670600-169678000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
9	chr1:169671000-169675000	Genic enhancers	Monocytes-CD14+_RO01746	blood
10	chr1:169671200-169679400	Transcr. at gene 5' and 3'	Dnd41	blood
11	chr1:169672600-169677400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
12	chr1:169672600-169678000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:169672800-169674600	Weak transcription	Spleen	Spleen
14	chr1:169672800-169676000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr1:169673200-169674600	Transcr. at gene 5' and 3'	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:169673200-169676800	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
17	chr1:169673200-169678400	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
18	chr1:169673400-169674000	Enhancers	Thymus	Thymus
19	chr1:169673400-169674400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:169673400-169676600	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
21	chr1:169673600-169674000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:169673600-169674000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:169673600-169674000	Transcr. at gene 5' and 3'	Primary T killer memory cells from peripheral blood	blood
24	chr1:169673600-169674000	Enhancers	GM12878-XiMat	blood
25	chr1:169673600-169674200	Transcr. at gene 5' and 3'	Primary neutrophils fromperipheralblood	blood
26	chr1:169673600-169674400	Transcr. at gene 5' and 3'	Primary T killer naive cells fromperipheralblood	blood
27	chr1:169673600-169674400	Transcr. at gene 5' and 3'	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:169673800-169674800	Transcr. at gene 5' and 3'	Primary T helper cells fromperipheralblood	blood
29	chr1:169673800-169675800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood

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