Variant report

Variant	rs62117403
Chromosome Location	chr19:42324501-42324502
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:42209971..42212433-chr19:42322719..42325343,2	MCF-7	breast:
2	chr19:42296886..42297641-chr19:42324359..42325844,5	MCF-7	breast:
3	chr19:42313500..42317243-chr19:42321753..42325232,3	K562	blood:

Variant related genes	Relation type
ENSG00000007306	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10401370	0.86[EUR][1000 genomes]
rs10401528	0.86[EUR][1000 genomes]
rs10401928	0.89[EUR][1000 genomes]
rs10407206	0.91[EUR][1000 genomes]
rs10407619	0.90[EUR][1000 genomes]
rs10407797	0.92[EUR][1000 genomes]
rs10408367	0.89[EUR][1000 genomes]
rs10410918	0.89[EUR][1000 genomes]
rs10414823	0.90[EUR][1000 genomes]
rs10416824	0.90[EUR][1000 genomes]
rs10418100	0.85[EUR][1000 genomes]
rs10419111	0.87[EUR][1000 genomes]
rs10419827	0.85[EUR][1000 genomes]
rs10426243	0.85[EUR][1000 genomes]
rs10500284	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12979253	0.88[EUR][1000 genomes]
rs1811564	0.89[EUR][1000 genomes]
rs1870093	0.86[EUR][1000 genomes]
rs2008798	0.90[EUR][1000 genomes]
rs2008808	0.87[EUR][1000 genomes]
rs2199829	0.89[EUR][1000 genomes]
rs2199830	0.90[EUR][1000 genomes]
rs28821622	0.89[EUR][1000 genomes]
rs28824227	0.90[EUR][1000 genomes]
rs28847113	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34819714	0.84[EUR][1000 genomes]
rs3795022	0.89[EUR][1000 genomes]
rs4480913	0.89[EUR][1000 genomes]
rs6508998	0.89[EUR][1000 genomes]
rs6508999	0.89[EUR][1000 genomes]
rs6509000	0.88[EUR][1000 genomes]
rs7251154	0.82[EUR][1000 genomes]
rs7251336	0.86[EUR][1000 genomes]
rs7251783	0.86[EUR][1000 genomes]
rs7251799	0.86[EUR][1000 genomes]
rs7251960	0.84[EUR][1000 genomes]
rs734107	0.90[EUR][1000 genomes]
rs734109	0.90[EUR][1000 genomes]
rs8099934	0.90[EUR][1000 genomes]
rs8100182	0.90[EUR][1000 genomes]
rs8106505	0.90[EUR][1000 genomes]
rs8110199	0.90[EUR][1000 genomes]
rs8113283	0.88[EUR][1000 genomes]
rs8113538	0.89[EUR][1000 genomes]
rs8113641	0.89[EUR][1000 genomes]
rs8113720	0.89[EUR][1000 genomes]
rs8113741	0.89[EUR][1000 genomes]
rs8113813	0.89[EUR][1000 genomes]
rs899662	0.89[EUR][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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv960847	chr19:42319253-42339596	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62117403	RABAC1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42322800-42324600	Enhancers	Primary neutrophils fromperipheralblood	blood

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