Variant report

No.	Distal block	Cell Line	Cell type
1	chr13:97789069..97794606-chr13:97796016..97800489,5	K562	blood:
2	chr13:97793649..97795166-chr13:97797379..97799703,2	MCF-7	breast:
3	chr13:97791984..97795803-chr13:97797601..97802176,4	K562	blood:

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10161888	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16953867	0.87[EUR][1000 genomes]
rs16953933	0.87[EUR][1000 genomes]
rs3891672	0.81[EUR][1000 genomes]
rs3904139	0.87[EUR][1000 genomes]
rs55669814	0.87[EUR][1000 genomes]
rs55736008	0.87[EUR][1000 genomes]
rs56331763	0.84[EUR][1000 genomes]
rs59939527	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7317617	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7326329	0.87[EUR][1000 genomes]
rs7326670	0.84[EUR][1000 genomes]
rs7327054	0.87[EUR][1000 genomes]
rs7327112	0.87[EUR][1000 genomes]
rs7329164	0.84[EUR][1000 genomes]
rs7332935	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7334833	0.90[EUR][1000 genomes]
rs7335512	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7339217	0.84[EUR][1000 genomes]
rs73553557	0.87[EUR][1000 genomes]
rs73553593	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73555705	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7358964	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs74107562	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7983752	0.87[EUR][1000 genomes]
rs7984448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7988970	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9284175	0.87[EUR][1000 genomes]
rs947452	0.90[EUR][1000 genomes]
rs9582110	0.84[EUR][1000 genomes]
rs9584506	0.84[EUR][1000 genomes]
rs9652111	0.81[EUR][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	nsv1053686	chr13:97771607-97802296	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	4 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	chr13:97787000-97799000	Weak transcription	Lung	lung
2	chr13:97795000-97801200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr13:97795200-97799000	Weak transcription	Right Atrium	heart
4	chr13:97795600-97800600	Weak transcription	K562	blood
5	chr13:97795800-97798800	Weak transcription	Fetal Lung	lung
6	chr13:97798000-97799200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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