Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74256949..74258669-chr4:74264666..74267423,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10030080	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10032380	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12510553	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13106620	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849267	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16849364	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16849366	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28821191	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34681098	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34787727	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35215741	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3822100	0.83[EUR][1000 genomes]
rs4364229	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4446279	0.85[EUR][1000 genomes]
rs4591567	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4640638	0.85[EUR][1000 genomes]
rs667	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6829532	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6829551	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6834059	0.85[EUR][1000 genomes]
rs6836787	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6845493	0.93[EUR][1000 genomes];0.88[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	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr4:74256400-74260200	Enhancers	HepG2	liver
2	chr4:74256600-74258000	Enhancers	Liver	Liver
3	chr4:74257600-74257800	Enhancers	Fetal Intestine Large	intestine
4	chr4:74257600-74258000	Enhancers	Fetal Intestine Small	intestine

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