Variant report

Variant	rs272280
Chromosome Location	chr13:64629409-64629410
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:64573569..64576340-chr13:64627433..64629862,2	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs183864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs198980	0.85[AMR][1000 genomes]
rs269556	0.88[AFR][1000 genomes]
rs269559	0.88[AFR][1000 genomes]
rs269561	0.88[AFR][1000 genomes]
rs269562	0.88[AFR][1000 genomes]
rs269566	0.85[AMR][1000 genomes]
rs269567	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269571	0.85[AMR][1000 genomes]
rs269573	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269576	0.85[AMR][1000 genomes]
rs269577	0.85[AMR][1000 genomes]
rs269579	0.98[AFR][1000 genomes]
rs269613	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269616	0.85[AMR][1000 genomes]
rs269617	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269620	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269622	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269623	0.85[AMR][1000 genomes]
rs269624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269642	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269644	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs269645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs272346	0.88[AFR][1000 genomes]
rs272361	0.88[AFR][1000 genomes]
rs374928	0.88[AFR][1000 genomes]
rs377326	0.85[AMR][1000 genomes]
rs391161	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs396677	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs399392	0.88[AFR][1000 genomes]
rs415464	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs416898	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs425019	0.83[AFR][1000 genomes]
rs428277	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs434464	0.88[AFR][1000 genomes]
rs450390	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900332	chr13:64411616-64856866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv561964	chr13:64412839-64967458	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1044946	chr13:64419179-64937470	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1038291	chr13:64424127-64937470	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1047229	chr13:64424127-64962138	Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1037078	chr13:64424251-64937470	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1036164	chr13:64425528-64933932	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv516171	chr13:64432922-64936243	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1041541	chr13:64446654-64913526	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv541807	chr13:64446654-64913526	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv994983	chr13:64446655-64913525	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv916348	chr13:64446759-64913520	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv455915	chr13:64455165-64933618	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv561966	chr13:64455165-64933618	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv482659	chr13:64457132-64634096	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	esv2763030	chr13:64545539-64719372	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv832634	chr13:64583792-64737416	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv430577	chr13:64602899-65034099	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	nsv1041341	chr13:64606955-64639095	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
22	nsv977252	chr13:64622723-64641183	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64627600-64631400	Weak transcription	K562	blood
2	chr13:64627800-64629800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr13:64627800-64630200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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