Variant report

Variant	rs72948021
Chromosome Location	chr1:72262796-72262797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10789328	0.99[ASN][1000 genomes]
rs10789330	0.99[ASN][1000 genomes]
rs11209837	0.93[ASN][1000 genomes]
rs11209840	0.96[ASN][1000 genomes]
rs11209842	0.97[ASN][1000 genomes]
rs11584866	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12023733	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12023757	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12024388	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12030035	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12039538	0.84[AMR][1000 genomes]
rs12041607	0.80[AMR][1000 genomes]
rs12048869	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12731898	0.99[ASN][1000 genomes]
rs1459795	0.96[ASN][1000 genomes]
rs1459796	0.89[EUR][1000 genomes]
rs1459801	0.99[ASN][1000 genomes]
rs1491198	0.99[ASN][1000 genomes]
rs17091758	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1817805	0.99[ASN][1000 genomes]
rs1844788	0.99[ASN][1000 genomes]
rs1870523	0.93[ASN][1000 genomes]
rs1870524	0.93[ASN][1000 genomes]
rs1870525	0.93[ASN][1000 genomes]
rs2061495	0.99[ASN][1000 genomes]
rs2125775	0.97[ASN][1000 genomes]
rs2125776	0.92[ASN][1000 genomes]
rs2125777	0.97[ASN][1000 genomes]
rs2169096	0.99[ASN][1000 genomes]
rs4649945	0.96[ASN][1000 genomes]
rs4649947	0.99[ASN][1000 genomes]
rs4649949	0.99[ASN][1000 genomes]
rs4649950	0.99[ASN][1000 genomes]
rs4650121	0.99[ASN][1000 genomes]
rs4650122	0.99[ASN][1000 genomes]
rs57227393	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57839383	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59851000	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6424442	0.80[AMR][1000 genomes]
rs6424447	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6424448	0.99[ASN][1000 genomes]
rs6671557	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6697370	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6701156	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72944111	0.80[AMR][1000 genomes]
rs72944128	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72944129	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72944192	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72946013	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72946022	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72946034	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7520452	0.93[ASN][1000 genomes]
rs7528030	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7531512	0.80[AMR][1000 genomes]
rs7541406	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7546909	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9662397	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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
6	nsv817447	chr1:72098815-72558020	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1008210	chr1:72099161-72374197	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv830181	chr1:72155983-72296578	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv916783	chr1:72196061-72707953	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1007910	chr1:72247302-72543998	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr1:72256400-72263000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:72258200-72262800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:72261800-72263200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:72262200-72263000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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