Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:103232129..103235431-chr7:103236152..103239545,4	K562	blood:
2	chr7:103218935..103220580-chr7:103231967..103234763,2	K562	blood:
3	chr7:103224194..103227224-chr7:103230117..103233349,3	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12533612	0.91[AMR][1000 genomes]
rs12539423	0.91[AMR][1000 genomes]
rs17153784	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17153873	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17154011	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17154172	0.91[AMR][1000 genomes]
rs2072402	0.82[ASN][1000 genomes]
rs2072403	0.82[ASN][1000 genomes]
rs2072404	0.82[ASN][1000 genomes]
rs2073552	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2073553	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2073554	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2075042	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2240964	0.82[ASN][1000 genomes]
rs2299339	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2299351	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2299352	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3025970	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs34196791	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs362685	0.91[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs362704	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3757739	0.91[AMR][1000 genomes]
rs3757740	0.91[AMR][1000 genomes]
rs3757741	0.91[AMR][1000 genomes]
rs3808022	0.91[AMR][1000 genomes]
rs3808023	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3808025	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3808028	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103206000-103243400	Weak transcription	K562	blood
2	chr7:103230400-103246200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:103232600-103234600	Strong transcription	HepG2	liver

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