Variant report

No.	Distal block	Cell Line	Cell type
1	chr1:166630170..166632723-chr1:166642991..166645828,4	K562	blood:
2	chr1:166630331..166631963-chr1:166643323..166644976,2	K562	blood:
3	chr1:166640499..166644852-chr1:166656070..166659050,4	K562	blood:
4	chr1:166642691..166644852-chr1:166657176..166659778,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10047082	0.89[ASN][1000 genomes]
rs10494466	0.87[ASN][1000 genomes]
rs10800253	0.88[ASN][1000 genomes]
rs10918553	0.87[ASN][1000 genomes]
rs10918554	0.89[ASN][1000 genomes]
rs10918565	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11585016	0.89[ASN][1000 genomes]
rs12022833	0.85[ASN][1000 genomes]
rs12074945	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12082938	0.89[ASN][1000 genomes]
rs12406568	0.89[ASN][1000 genomes]
rs17472904	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2119900	0.83[EUR][1000 genomes]
rs3856217	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3904701	0.88[ASN][1000 genomes]
rs4068473	0.88[ASN][1000 genomes]
rs4090281	0.89[ASN][1000 genomes]
rs4393133	0.88[ASN][1000 genomes]
rs4657571	0.85[EUR][1000 genomes]
rs4657581	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs505012	0.81[ASN][1000 genomes]
rs563206	0.87[ASN][1000 genomes]
rs566841	0.87[ASN][1000 genomes]
rs6676923	0.81[EUR][1000 genomes]
rs7517690	0.89[ASN][1000 genomes]
rs7531612	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv2757759	chr1:166491879-166650985	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2758975	chr1:166491879-166650985	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2752389	chr1:166625342-166706342	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166644000-166644800	Enhancers	K562	blood

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