Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:103302157..103305081-chr7:103307428..103309222,2	K562	blood:
2	chr7:103297558..103299544-chr7:103301065..103303822,2	K562	blood:
3	chr7:103302444..103304759-chr7:103358804..103361595,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1012064	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1012065	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10261317	0.81[ASN][1000 genomes]
rs10487161	0.82[ASN][1000 genomes]
rs10953389	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1122672	0.82[ASN][1000 genomes]
rs12668066	0.82[ASN][1000 genomes]
rs12671936	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12672672	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12674323	0.82[ASN][1000 genomes]
rs17154114	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1860686	0.89[AFR][1000 genomes]
rs2017179	0.87[ASN][1000 genomes]
rs2191707	0.81[ASN][1000 genomes]
rs2215537	0.81[ASN][1000 genomes]
rs2240965	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2299358	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3025967	0.82[ASN][1000 genomes]
rs3808021	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67423770	0.86[AFR][1000 genomes]
rs67811550	0.83[AFR][1000 genomes]
rs67823578	0.84[AFR][1000 genomes]
rs977638	0.82[ASN][1000 genomes]
rs977639	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831085	chr7:103140672-103342388	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1835816	chr7:103255144-103354223	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv933440	chr7:103301959-103312307	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv933934	chr7:103301959-103322483	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103298200-103305000	Enhancers	HepG2	liver
2	chr7:103300600-103303200	Enhancers	Hela-S3	cervix
3	chr7:103303000-103304400	Enhancers	K562	blood

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