Variant report

Variant	rs61299618
Chromosome Location	chr1:175560465-175560466
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10158732	0.80[AMR][1000 genomes]
rs10913007	0.80[AMR][1000 genomes]
rs10913008	0.80[AMR][1000 genomes]
rs10913009	0.80[AMR][1000 genomes]
rs10913014	0.86[AMR][1000 genomes]
rs10913024	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913025	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913026	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913027	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10913028	0.98[EUR][1000 genomes]
rs12065732	0.88[EUR][1000 genomes]
rs12093333	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12240118	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12240159	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12240162	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12565695	0.80[AMR][1000 genomes]
rs16848627	0.80[AMR][1000 genomes]
rs16848635	0.80[AMR][1000 genomes]
rs16848649	0.80[AMR][1000 genomes]
rs16848698	0.90[AMR][1000 genomes]
rs16848703	0.90[AMR][1000 genomes]
rs16848729	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16848734	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16848737	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16848739	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57091017	1.00[EUR][1000 genomes]
rs57107679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58376805	0.80[AMR][1000 genomes]
rs59377605	0.80[AMR][1000 genomes]
rs59686392	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59874028	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60808618	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61473560	0.80[AMR][1000 genomes]
rs6688098	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6690188	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6702143	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7538156	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9286909	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999586	chr1:175428957-175765789	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1014015	chr1:175430199-175752187	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1012012	chr1:175430199-175760752	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1000135	chr1:175430199-175765789	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1008727	chr1:175430808-175752725	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1008620	chr1:175430808-175760752	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv527256	chr1:175430855-175582250	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv466072	chr1:175430855-175739003	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv548243	chr1:175430855-175739003	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv528975	chr1:175430855-175757242	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv466083	chr1:175430855-175757242	Active TSS Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv548244	chr1:175430855-175757242	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv548245	chr1:175430855-175772378	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv1004585	chr1:175436519-175739951	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv998119	chr1:175436519-175760752	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv948460	chr1:175439176-175751385	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv1011962	chr1:175440153-175760752	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	esv33328	chr1:175446583-175910001	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
19	nsv915955	chr1:175448830-175704923	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
20	nsv998327	chr1:175448846-175704803	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	nsv535211	chr1:175448846-175704803	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
22	nsv1001391	chr1:175448870-175728998	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
23	nsv535212	chr1:175448870-175728998	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:175559600-175561000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:175559600-175561200	Enhancers	K562	blood
3	chr1:175559600-175561600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:175559800-175560800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr1:175559800-175560800	Enhancers	Lung	lung
6	chr1:175559800-175560800	Enhancers	Spleen	Spleen
7	chr1:175559800-175561000	Enhancers	Primary hematopoietic stem cells	blood
8	chr1:175559800-175561000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:175560000-175561000	Enhancers	Brain Germinal Matrix	brain
10	chr1:175560000-175566200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr1:175560200-175560600	Enhancers	Right Atrium	heart
12	chr1:175560200-175560800	Enhancers	Pancreas	Pancrea
13	chr1:175560200-175561000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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