Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:138113307..138115089-chr7:138144254..138145776,2	K562	blood:

Variant related genes	Relation type
ENSG00000122779	Chromatin interaction

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10248876	0.86[ASN][1000 genomes]
rs10248991	0.86[ASN][1000 genomes]
rs10249020	0.86[ASN][1000 genomes]
rs10249638	0.86[ASN][1000 genomes]
rs2353345	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2353348	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4367480	0.81[ASN][1000 genomes]
rs4574789	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4620232	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4626544	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4992351	0.82[ASN][1000 genomes]
rs55792279	0.82[ASN][1000 genomes]
rs6467769	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6467772	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6947999	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6951998	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6953860	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6959223	0.81[ASN][1000 genomes]
rs6962241	0.87[ASN][1000 genomes]
rs6962854	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6964218	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6968570	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6980108	0.87[ASN][1000 genomes]
rs7785428	0.82[ASN][1000 genomes]
rs7793703	0.85[AMR][1000 genomes];0.89[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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831153	chr7:138078179-138265648	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr7:138110200-138113800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:138112600-138117000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr7:138113000-138115200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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