Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27470047..27472027-chr7:27474314..27477072,2	K562	blood:
2	chr7:27468218..27471547-chr7:27472130..27475962,5	K562	blood:

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

rs_ID	r²[population]
rs10242634	0.84[ASN][1000 genomes]
rs10252511	0.86[ASN][1000 genomes]
rs10252636	0.86[ASN][1000 genomes]
rs10268623	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10269160	0.85[ASN][1000 genomes]
rs10272561	0.82[ASN][1000 genomes]
rs10276795	0.86[ASN][1000 genomes]
rs1112620	0.86[ASN][1000 genomes]
rs11763775	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12540319	0.81[ASN][1000 genomes]
rs1524522	0.86[ASN][1000 genomes]
rs1989910	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2074340	0.88[ASN][1000 genomes]
rs2074341	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28418930	0.88[ASN][1000 genomes]
rs28625460	0.86[ASN][1000 genomes]
rs3915086	0.86[ASN][1000 genomes]
rs3915089	0.85[ASN][1000 genomes]
rs4141138	0.87[ASN][1000 genomes]
rs4722700	0.85[ASN][1000 genomes]
rs4722701	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4722702	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4722706	0.82[ASN][1000 genomes]
rs4722707	0.86[ASN][1000 genomes]
rs56843699	0.86[ASN][1000 genomes]
rs62454789	0.87[ASN][1000 genomes]
rs62454790	0.87[ASN][1000 genomes]
rs6953785	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs757141	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7786854	0.84[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	nsv830930	chr7:27395838-27587355	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27463400-27471800	Weak transcription	Spleen	Spleen
2	chr7:27465200-27472200	Weak transcription	Stomach Mucosa	stomach
3	chr7:27466200-27473800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:27469600-27472800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:27469800-27473000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:27470000-27472800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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