Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:129619552..129621316-chr7:129689719..129692447,2	K562	blood:
2	chr7:129617281..129619116-chr7:129619562..129624001,4	K562	blood:

Variant related genes	Relation type
ENSG00000091732	Chromatin interaction

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10231719	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs10246708	1.00[ASN][1000 genomes]
rs10247295	1.00[ASN][1000 genomes]
rs10271407	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2177773	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28563772	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4580987	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4606000	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56990459	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs59117588	0.81[EUR][1000 genomes]
rs62489404	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs6467274	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6945757	1.00[ASN][1000 genomes]
rs6949020	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6959601	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975656	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975965	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7778194	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7805545	1.00[ASN][1000 genomes]
rs7805829	1.00[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	nsv831129	chr7:129525406-129702477	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:129598800-129629600	Weak transcription	Right Atrium	heart
2	chr7:129614600-129623800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:129615600-129623800	Weak transcription	Hela-S3	cervix
4	chr7:129617800-129622200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:129618000-129623400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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