Variant report

Variant	rs6866289
Chromosome Location	chr5:103496896-103496897
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:103493121..103495084-chr5:103495998..103498553,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11745594	0.98[ASN][1000 genomes]
rs11748709	1.00[ASN][1000 genomes]
rs1362697	0.80[ASN][1000 genomes]
rs1420866	0.83[ASN][1000 genomes]
rs1420867	0.83[ASN][1000 genomes]
rs1592631	0.82[ASN][1000 genomes]
rs1882562	0.83[ASN][1000 genomes]
rs1882563	0.83[ASN][1000 genomes]
rs1882564	0.83[ASN][1000 genomes]
rs1882565	0.83[ASN][1000 genomes]
rs1882566	0.83[ASN][1000 genomes]
rs1882567	0.83[ASN][1000 genomes]
rs1895020	0.82[ASN][1000 genomes]
rs1895021	0.80[ASN][1000 genomes]
rs1922488	0.98[ASN][1000 genomes]
rs1922505	0.83[ASN][1000 genomes]
rs1922506	0.83[ASN][1000 genomes]
rs1981768	0.83[ASN][1000 genomes]
rs1981769	0.83[ASN][1000 genomes]
rs1981770	0.83[ASN][1000 genomes]
rs1990749	0.83[ASN][1000 genomes]
rs2542083	0.83[ASN][1000 genomes]
rs2542084	0.83[ASN][1000 genomes]
rs2542085	0.83[ASN][1000 genomes]
rs2542086	0.83[ASN][1000 genomes]
rs2542087	0.83[ASN][1000 genomes]
rs2542088	0.83[ASN][1000 genomes]
rs2707404	0.83[ASN][1000 genomes]
rs2707405	0.84[ASN][1000 genomes]
rs2707406	0.83[ASN][1000 genomes]
rs2707407	0.83[ASN][1000 genomes]
rs2707408	0.82[ASN][1000 genomes]
rs2707409	0.82[ASN][1000 genomes]
rs2707410	0.83[ASN][1000 genomes]
rs2707411	0.83[ASN][1000 genomes]
rs2707412	0.83[ASN][1000 genomes]
rs2952550	0.83[ASN][1000 genomes]
rs2952551	0.83[ASN][1000 genomes]
rs35090102	1.00[ASN][1000 genomes]
rs3857362	1.00[ASN][1000 genomes]
rs4515272	0.99[ASN][1000 genomes]
rs4519904	0.87[ASN][1000 genomes]
rs4703287	0.83[ASN][1000 genomes]
rs4703288	0.84[ASN][1000 genomes]
rs4703289	0.83[ASN][1000 genomes]
rs6596566	0.87[ASN][1000 genomes]
rs6861405	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6874424	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025859	chr5:102744479-103710290	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537833	chr5:102744479-103710290	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv882524	chr5:103237745-104019292	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1019939	chr5:103380722-103770101	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv537836	chr5:103380722-103770101	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1033278	chr5:103383207-103773361	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv462330	chr5:103406680-103533884	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv599201	chr5:103406680-103533884	Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv599205	chr5:103478518-103614650	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv531969	chr5:103482070-104249804	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	esv2758008	chr5:103483784-103633568	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	esv2759362	chr5:103483784-103633568	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1033485	chr5:103487985-103589765	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103496600-103497000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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