Variant report

Variant	rs3007693
Chromosome Location	chr1:151932375-151932376
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	chr1:151925413..151928425-chr1:151930738..151934740,3	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1038746	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1038748	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1387834	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1387835	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1473493	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1473494	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1473495	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1490190	0.85[AFR][1000 genomes]
rs1490191	0.86[AMR][1000 genomes]
rs1532132	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1552605	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1552607	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1602245	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1602246	0.88[EUR][1000 genomes]
rs1602248	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17583707	0.83[AMR][1000 genomes]
rs1826170	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1826171	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1826172	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1873311	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2087550	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2338018	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932563	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932564	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932578	0.80[AFR][1000 genomes]
rs2932584	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2932585	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2932588	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932591	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932592	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932595	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932596	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2932597	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999509	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999511	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2999514	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999515	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999518	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999519	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999520	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999522	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999524	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999525	0.86[EUR][1000 genomes]
rs2999527	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999529	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2999530	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2999558	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3007682	0.80[AFR][1000 genomes]
rs3007692	0.89[AMR][1000 genomes]
rs3007699	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3007700	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3007701	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3007704	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34370890	0.83[AMR][1000 genomes]
rs61113720	0.83[AMR][1000 genomes]
rs971888	0.80[AMR][1000 genomes];0.86[EUR][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	nsv1007097	chr1:151832796-152227977	Strong transcription Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
2	nsv1012327	chr1:151835544-152200890	Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
3	nsv535159	chr1:151835544-152200890	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
4	nsv547852	chr1:151843044-151955230	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	nsv872441	chr1:151850072-152034430	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	191 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151928000-151933000	Weak transcription	Fetal Intestine Small	intestine
2	chr1:151930800-151940800	Weak transcription	NHDF-Ad	bronchial
3	chr1:151931600-151934000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:151931800-151935200	Weak transcription	Hela-S3	cervix
5	chr1:151932000-151933000	Weak transcription	Monocytes-CD14+_RO01746	blood

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