Variant report

Variant	rs1511036
Chromosome Location	chr18:30249433-30249434
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:30156679..30157193-chr18:30249087..30249714,2	MCF-7	breast:
2	chr18:30155938..30156890-chr18:30249254..30250445,9	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11081778	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1125317	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11875943	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12607749	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12957148	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12961515	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13381681	1.00[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1523580	0.87[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1523581	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1523582	0.95[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1523584	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1523585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523586	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523587	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523589	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs162418	0.94[JPT][hapmap]
rs162419	0.94[JPT][hapmap]
rs162420	0.85[CHB][hapmap];0.93[JPT][hapmap]
rs162421	0.80[CHB][hapmap];0.94[JPT][hapmap]
rs1846013	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1980034	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1980035	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1980036	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2421639	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28417613	0.80[EUR][1000 genomes]
rs2901486	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs330296	0.91[JPT][hapmap]
rs330297	0.94[JPT][hapmap]
rs330298	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs330299	0.94[JPT][hapmap]
rs330301	0.94[JPT][hapmap]
rs330303	0.81[CHB][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap]
rs330304	0.81[CHB][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap]
rs330305	0.83[GIH][hapmap];0.87[JPT][hapmap]
rs330330	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs330333	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35555190	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4344834	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs59707505	0.84[EUR][1000 genomes]
rs7241043	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8092564	0.94[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap];0.88[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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30248800-30249600	Enhancers	Brain Germinal Matrix	brain
2	chr18:30248800-30250000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr18:30249400-30252000	Weak transcription	Fetal Brain Male	brain

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