Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103308135..103310700-chr7:103389205..103391721,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10487167	1.00[CEU][hapmap];0.84[CHD][hapmap];0.83[GIH][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs17153784	0.82[CEU][hapmap]
rs17153873	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs17154011	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs17154172	0.82[CEU][hapmap]
rs17154414	0.82[CEU][hapmap];0.83[GIH][hapmap];0.84[MEX][hapmap];0.81[YRI][hapmap]
rs17155063	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs17155341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2072402	0.82[CEU][hapmap]
rs2072403	0.82[CEU][hapmap]
rs2072404	0.82[CEU][hapmap]
rs2073553	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs2075042	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs2237634	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3025970	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs362685	0.82[CEU][hapmap]
rs3757737	0.82[CEU][hapmap]
rs3808022	0.82[CEU][hapmap]
rs3808023	0.82[CEU][hapmap]
rs3808025	0.82[CEU][hapmap]
rs3808028	0.82[CEU][hapmap]
rs7805831	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7806181	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[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	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	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
3	nsv524101	chr7:103391042-103391409	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103390000-103434000	Weak transcription	K562	blood
2	chr7:103391000-103393400	Strong transcription	HepG2	liver

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