Variant report

Variant	rs73765283
Chromosome Location	chr6:113897798-113897799
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SETDB1	chr6:113897417-113897883	U2OS	brain:	n/a	n/a

Variant related genes	Relation type
ENSG00000218208	TF binding region

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1481432	1.00[EUR][1000 genomes]
rs1585973	1.00[EUR][1000 genomes]
rs1600767	1.00[EUR][1000 genomes]
rs17075218	1.00[EUR][1000 genomes]
rs17075221	1.00[EUR][1000 genomes]
rs1904994	1.00[EUR][1000 genomes]
rs1982686	1.00[EUR][1000 genomes]
rs2493884	1.00[EUR][1000 genomes]
rs2493885	1.00[EUR][1000 genomes]
rs2493891	1.00[EUR][1000 genomes]
rs3963300	1.00[EUR][1000 genomes]
rs4337960	1.00[EUR][1000 genomes]
rs531979	1.00[EUR][1000 genomes]
rs547797	1.00[EUR][1000 genomes]
rs549875	1.00[EUR][1000 genomes]
rs56303196	1.00[EUR][1000 genomes]
rs57194334	1.00[EUR][1000 genomes]
rs58875635	1.00[EUR][1000 genomes]
rs58891033	1.00[EUR][1000 genomes]
rs59844934	1.00[EUR][1000 genomes]
rs59950054	1.00[EUR][1000 genomes]
rs60295562	1.00[EUR][1000 genomes]
rs60504130	1.00[EUR][1000 genomes]
rs61320559	1.00[EUR][1000 genomes]
rs6913809	1.00[EUR][1000 genomes]
rs6926011	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6942149	1.00[EUR][1000 genomes]
rs73531703	1.00[EUR][1000 genomes]
rs73547891	1.00[EUR][1000 genomes]
rs73765224	1.00[EUR][1000 genomes]
rs73765225	1.00[EUR][1000 genomes]
rs73765247	1.00[EUR][1000 genomes]
rs73765256	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765261	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765266	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765267	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765271	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765272	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73765273	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7745709	1.00[EUR][1000 genomes]
rs7749447	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7752840	1.00[EUR][1000 genomes]
rs7753869	1.00[EUR][1000 genomes]
rs7754686	1.00[EUR][1000 genomes]
rs7758523	1.00[EUR][1000 genomes]
rs7759659	1.00[EUR][1000 genomes]
rs7762969	1.00[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	nsv916294	chr6:113518489-113904305	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113895800-113900400	Weak transcription	Stomach Mucosa	stomach
2	chr6:113896000-113900200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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