Variant report

Variant	rs7806733
Chromosome Location	chr7:118263265-118263266
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1120921	0.81[EUR][1000 genomes]
rs1120922	0.81[EUR][1000 genomes]
rs11560382	0.86[EUR][1000 genomes]
rs11765778	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11772018	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12668697	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13237572	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13241168	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1397325	0.81[EUR][1000 genomes]
rs1510502	0.87[EUR][1000 genomes]
rs1588447	0.87[EUR][1000 genomes]
rs1721228	0.86[EUR][1000 genomes]
rs1916710	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1916713	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2214150	0.81[EUR][1000 genomes]
rs2248782	0.81[EUR][1000 genomes]
rs2402397	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2402398	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2402399	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2521214	0.81[EUR][1000 genomes]
rs2521215	0.81[EUR][1000 genomes]
rs2521216	0.81[EUR][1000 genomes]
rs2521217	0.81[EUR][1000 genomes]
rs2665760	0.81[EUR][1000 genomes]
rs2665763	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2665764	0.81[EUR][1000 genomes]
rs2665765	0.81[EUR][1000 genomes]
rs2665766	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2665769	0.81[EUR][1000 genomes]
rs2665770	0.87[EUR][1000 genomes]
rs2689753	0.81[EUR][1000 genomes]
rs2689754	0.81[EUR][1000 genomes]
rs2689755	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2689756	0.80[EUR][1000 genomes]
rs2689757	0.81[EUR][1000 genomes]
rs2689758	0.81[EUR][1000 genomes]
rs304521	0.81[EUR][1000 genomes]
rs304522	0.81[EUR][1000 genomes]
rs304524	0.86[EUR][1000 genomes]
rs304534	0.84[EUR][1000 genomes]
rs304535	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4582494	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62468656	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62468657	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62468658	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6466668	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6466669	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6466671	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6951273	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6967347	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6968493	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6972496	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7797235	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7797750	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr7:118262400-118263800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:118262800-118264000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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