Variant report

Variant	rs73081485
Chromosome Location	chr1:215663031-215663032
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:215653919..215659650-chr1:215659919..215663792,9	MCF-7	breast:
2	chr1:215646817..215649143-chr1:215661987..215663671,2	MCF-7	breast:
3	chr1:215656949..215659189-chr1:215661543..215664424,2	K562	blood:
4	chr1:215598355..215599119-chr1:215661939..215663301,3	MCF-7	breast:
5	chr1:215598452..215599119-chr1:215662801..215663769,2	MCF-7	breast:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs12740635	1.00[AFR][1000 genomes]
rs56728838	1.00[AFR][1000 genomes]
rs56849908	1.00[AFR][1000 genomes]
rs57179404	1.00[AFR][1000 genomes]
rs57420199	1.00[AFR][1000 genomes]
rs57432920	1.00[AFR][1000 genomes]
rs57772200	1.00[AFR][1000 genomes]
rs57782276	1.00[AFR][1000 genomes]
rs58393812	1.00[AFR][1000 genomes]
rs58616406	1.00[AFR][1000 genomes]
rs58760828	1.00[AFR][1000 genomes]
rs58896701	1.00[AFR][1000 genomes]
rs59762493	1.00[AFR][1000 genomes]
rs60134994	1.00[AFR][1000 genomes]
rs60365921	1.00[AFR][1000 genomes]
rs60987968	1.00[AFR][1000 genomes]
rs61080723	1.00[AFR][1000 genomes]
rs61490597	1.00[AFR][1000 genomes]
rs61568482	1.00[AFR][1000 genomes]
rs73081431	1.00[AFR][1000 genomes]
rs73081436	1.00[AFR][1000 genomes]
rs73081438	1.00[AFR][1000 genomes]
rs73081440	1.00[AFR][1000 genomes]
rs73081445	1.00[AFR][1000 genomes]
rs73081450	1.00[AFR][1000 genomes]
rs73081451	1.00[AFR][1000 genomes]
rs73081453	1.00[AFR][1000 genomes]
rs73081455	1.00[AFR][1000 genomes]
rs73081459	1.00[AFR][1000 genomes]
rs73081462	1.00[AFR][1000 genomes]
rs73081464	1.00[AFR][1000 genomes]
rs73081465	1.00[AFR][1000 genomes]
rs73081466	1.00[AFR][1000 genomes]
rs73081469	1.00[AFR][1000 genomes]
rs73081470	1.00[AFR][1000 genomes]
rs73081472	1.00[AFR][1000 genomes]
rs73081474	1.00[AFR][1000 genomes]
rs73081477	1.00[AFR][1000 genomes]
rs73081479	1.00[AFR][1000 genomes]
rs73081482	1.00[AFR][1000 genomes]
rs73081486	1.00[AFR][1000 genomes]
rs73081487	1.00[AFR][1000 genomes]
rs73081489	1.00[AFR][1000 genomes]
rs73081490	1.00[AFR][1000 genomes]
rs73081491	1.00[AFR][1000 genomes]
rs73081499	1.00[AFR][1000 genomes]
rs73081501	1.00[AFR][1000 genomes]
rs73083404	1.00[AFR][1000 genomes]
rs73083406	1.00[AFR][1000 genomes]
rs73083409	1.00[AFR][1000 genomes]
rs73083410	0.90[AFR][1000 genomes]
rs73083413	1.00[AFR][1000 genomes]
rs73100128	1.00[AFR][1000 genomes]
rs73100141	1.00[AFR][1000 genomes]
rs73100142	1.00[AFR][1000 genomes]
rs73100147	1.00[AFR][1000 genomes]
rs73100151	1.00[AFR][1000 genomes]
rs73100153	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832537	chr1:215509026-215705105	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv1796390	chr1:215561548-215799074	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1014266	chr1:215573051-215730838	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv947159	chr1:215645387-215673199	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215648800-215663200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:215659800-215663600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:215660000-215663600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:215662000-215663400	Enhancers	Osteobl	bone
5	chr1:215662600-215664200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:215662800-215664200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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