Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:97831848..97833511-chr13:97836246..97838182,2	K562	blood:
2	chr13:97829083..97831662-chr13:97836176..97837942,2	K562	blood:

Variant related genes	Relation type
ENSG00000233124	Chromatin interaction

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

rs_ID	r²[population]
rs10161888	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16953867	0.80[EUR][1000 genomes]
rs16953933	0.93[EUR][1000 genomes]
rs3904139	0.93[EUR][1000 genomes]
rs55669814	0.80[EUR][1000 genomes]
rs55736008	0.80[EUR][1000 genomes]
rs56331763	0.90[EUR][1000 genomes]
rs7317617	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7326329	0.93[EUR][1000 genomes]
rs7327054	0.93[EUR][1000 genomes]
rs7327112	0.80[EUR][1000 genomes]
rs7332122	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7332935	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7334833	0.97[EUR][1000 genomes]
rs7335512	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73553557	0.80[EUR][1000 genomes]
rs73553593	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73555705	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7358964	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs74107562	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7983752	0.93[EUR][1000 genomes]
rs7984448	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7988970	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9284175	0.81[EUR][1000 genomes]
rs947452	0.84[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	nsv1137	chr13:97803474-97848814	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 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	chr13:97830200-97843400	Weak transcription	Spleen	Spleen
2	chr13:97832600-97837800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:97832800-97840400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr13:97836400-97841200	Enhancers	Placenta	Placenta
5	chr13:97837200-97839600	Weak transcription	Ovary	ovary

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