Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:95549239..95551783-chr1:95557722..95560296,2	K562	blood:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11165283	0.81[ASN][1000 genomes]
rs12119383	0.92[AMR][1000 genomes]
rs12119469	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12119701	0.83[ASN][1000 genomes]
rs12121738	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12123807	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12124097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12126245	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12136552	0.84[AMR][1000 genomes]
rs12137333	0.83[ASN][1000 genomes]
rs12139069	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12141083	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12142619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4245669	0.82[ASN][1000 genomes]
rs4847374	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4847375	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4847376	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs58602136	0.83[ASN][1000 genomes]
rs61772641	0.83[ASN][1000 genomes]
rs71483843	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7527765	0.83[ASN][1000 genomes]
rs7532763	0.83[ASN][1000 genomes]
rs7551281	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9787257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9787343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830636	chr1:95495849-95703126	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95554200-95564000	Weak transcription	Osteobl	bone
2	chr1:95558400-95562400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:95559000-95561000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:95559200-95560400	Enhancers	K562	blood
5	chr1:95559200-95561600	Weak transcription	A549	lung
6	chr1:95559400-95560400	Weak transcription	HepG2	liver
7	chr1:95560000-95560800	Enhancers	Fetal Heart	heart

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