Variant report

No.	Distal block	Cell Line	Cell type
1	chr4:110134315..110136735-chr4:110139001..110141315,2	K562	blood:
2	chr4:110133443..110135815-chr4:110139815..110141700,2	K562	blood:
3	chr4:110136926..110139311-chr4:110139884..110142095,2	K562	blood:

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

rs_ID	r²[population]
rs10488876	0.83[EUR][1000 genomes]
rs11932715	0.83[EUR][1000 genomes]
rs11934385	0.83[EUR][1000 genomes]
rs11943443	0.83[EUR][1000 genomes]
rs11946089	0.83[EUR][1000 genomes]
rs17040080	0.83[EUR][1000 genomes]
rs17040084	0.83[EUR][1000 genomes]
rs17040089	0.83[EUR][1000 genomes]
rs17040091	0.83[EUR][1000 genomes]
rs17040094	0.83[EUR][1000 genomes]
rs17040097	0.83[EUR][1000 genomes]
rs2007788	0.80[EUR][1000 genomes]
rs2007789	0.80[EUR][1000 genomes]
rs2158471	0.86[AFR][1000 genomes]
rs2189705	0.83[EUR][1000 genomes]
rs2526453	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2704101	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35702755	0.95[AFR][1000 genomes]
rs41395650	0.83[EUR][1000 genomes]
rs56844951	0.83[EUR][1000 genomes]
rs56946607	0.83[EUR][1000 genomes]
rs56982165	0.83[EUR][1000 genomes]
rs57810497	0.83[EUR][1000 genomes]
rs58325010	0.83[EUR][1000 genomes]
rs58848856	0.83[EUR][1000 genomes]
rs61659244	0.83[EUR][1000 genomes]
rs6533421	0.82[AFR][1000 genomes]
rs6825027	0.83[EUR][1000 genomes]
rs6825515	0.83[EUR][1000 genomes]
rs6825986	0.83[EUR][1000 genomes]
rs6842851	0.83[EUR][1000 genomes]
rs6843241	0.80[EUR][1000 genomes]
rs6843308	0.83[EUR][1000 genomes]
rs7656748	0.83[EUR][1000 genomes]
rs7662008	0.83[EUR][1000 genomes]
rs7675810	0.83[EUR][1000 genomes]
rs7681584	0.83[EUR][1000 genomes]
rs7686421	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7692009	0.83[EUR][1000 genomes]
rs7692026	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110137000-110145600	Weak transcription	Psoas Muscle	Psoas
2	chr4:110137600-110154400	Weak transcription	Hela-S3	cervix
3	chr4:110138400-110140600	Weak transcription	HUVEC	blood vessel

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