Variant report

Variant	rs227192
Chromosome Location	chr1:210210240-210210241
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1016479	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1099864	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17188183	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17188190	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2142857	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2205986	0.88[ASN][1000 genomes]
rs2205990	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs227185	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs227208	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs227214	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs227215	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2357211	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2451693	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2484029	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2494187	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2494188	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2743892	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61820393	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61827913	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61827915	0.85[ASN][1000 genomes]
rs61827917	0.85[ASN][1000 genomes]
rs61827918	0.85[ASN][1000 genomes]
rs61827920	0.85[ASN][1000 genomes]
rs61827921	0.85[ASN][1000 genomes]
rs6540571	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs719034	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72741075	0.82[ASN][1000 genomes]
rs846547	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs923561	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014034	chr1:209759648-210501731	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv873140	chr1:210068117-210335644	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1821002	chr1:210108473-210291476	ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr1:210193400-210221000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:210194800-210212400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:210195000-210221200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr1:210208200-210210400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:210209400-210212000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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