Variant report

Variant	rs35555190
Chromosome Location	chr18:30249782-30249783
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:30155938..30156890-chr18:30249254..30250445,9	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11081778	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1125317	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11875943	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12607749	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12957148	0.82[ASN][1000 genomes]
rs12961515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13381681	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1511036	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1523580	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1523581	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1523584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1523585	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1523586	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1523587	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1523589	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1846013	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1980034	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1980035	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1980036	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2421639	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28417613	0.91[EUR][1000 genomes]
rs2901486	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs330333	0.83[ASN][1000 genomes]
rs59707505	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7241043	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8092564	0.81[EUR][1000 genomes];0.83[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	nsv909526	chr18:30124311-30259109	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr18:30248800-30250000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr18:30249400-30252000	Weak transcription	Fetal Brain Male	brain

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