Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:127114890..127116879-chr7:127201699..127204076,2	K562	blood:
2	chr7:127203098..127205037-chr7:127222496..127224357,2	MCF-7	breast:
3	chr7:127201455..127203783-chr7:127214712..127216389,2	MCF-7	breast:
4	chr7:127201088..127203577-chr7:127205248..127208135,2	K562	blood:

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10265603	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10269701	0.83[ASN][1000 genomes]
rs10276671	0.87[AFR][1000 genomes]
rs10280804	0.88[AFR][1000 genomes]
rs10281056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10954161	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761988	1.00[ASN][1000 genomes]
rs11764631	0.98[ASN][1000 genomes]
rs11766383	0.87[AFR][1000 genomes]
rs11767380	1.00[ASN][1000 genomes]
rs1419430	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1557643	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17715255	1.00[ASN][1000 genomes]
rs17715285	1.00[ASN][1000 genomes]
rs1858785	0.95[AFR][1000 genomes]
rs34952162	0.83[ASN][1000 genomes]
rs35195581	1.00[ASN][1000 genomes]
rs4551267	0.91[ASN][1000 genomes]
rs4728072	1.00[ASN][1000 genomes]
rs4728073	1.00[ASN][1000 genomes]
rs4728075	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4731370	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55657491	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57867532	0.98[ASN][1000 genomes]
rs58894662	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62481345	0.83[ASN][1000 genomes]
rs6949899	0.81[CHB][hapmap]
rs6955138	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6970053	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs990032	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831122	chr7:127143207-127357885	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv1801682	chr7:127188972-127209982	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3336294	chr7:127203207-127205926	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127200600-127221400	Weak transcription	Pancreas	Pancrea
2	chr7:127203200-127214000	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr7:127203200-127214200	Weak transcription	Primary T cells from cord blood	blood
4	chr7:127203400-127220400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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