Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10493485	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10493486	0.85[AFR][1000 genomes]
rs10889921	0.97[EUR][1000 genomes]
rs11209800	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11209801	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11209806	0.85[AFR][1000 genomes]
rs12021677	0.96[EUR][1000 genomes]
rs12139658	0.92[EUR][1000 genomes]
rs12742274	0.93[EUR][1000 genomes]
rs12757229	0.90[EUR][1000 genomes]
rs1333998	0.92[EUR][1000 genomes]
rs1333999	0.92[EUR][1000 genomes]
rs1334000	0.92[EUR][1000 genomes]
rs1334001	0.92[EUR][1000 genomes]
rs1335223	0.92[EUR][1000 genomes]
rs1335224	0.89[EUR][1000 genomes]
rs1517752	0.89[EUR][1000 genomes]
rs17091560	0.85[AFR][1000 genomes]
rs1855647	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2184232	0.97[EUR][1000 genomes]
rs4649941	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6424431	0.92[EUR][1000 genomes]
rs6424432	0.92[EUR][1000 genomes]
rs6424433	0.92[EUR][1000 genomes]
rs6656539	0.92[EUR][1000 genomes]
rs6664443	0.90[EUR][1000 genomes]
rs6668345	0.89[EUR][1000 genomes]
rs6700555	0.90[EUR][1000 genomes]
rs7553565	0.92[EUR][1000 genomes]
rs928615	0.87[EUR][1000 genomes]
rs951950	0.89[EUR][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	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1007250	chr1:71998391-72350683	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv534992	chr1:71998391-72350683	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv948821	chr1:72049987-72477221	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1003446	chr1:72060680-72419918	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72054800-72071800	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:72055000-72075800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:72059200-72065000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:72059600-72067000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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