Variant report

Variant	rs6580661
Chromosome Location	chr12:48615118-48615119
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1074175	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10747532	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10783235	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10783240	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10783241	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10875780	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10875781	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10875796	0.81[ASN][1000 genomes]
rs10875797	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11168458	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs11168470	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168471	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168472	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168473	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168475	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168485	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168488	0.84[ASN][1000 genomes]
rs11168494	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11168513	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11168515	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11168532	0.80[ASN][1000 genomes]
rs12422306	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12423529	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12810029	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12815219	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12822431	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12824405	0.80[AMR][1000 genomes]
rs12831063	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1387261	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1844261	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2220459	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2291483	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2409002	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs35267282	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7136959	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs716176	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73116262	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv8971	chr12:48536526-48758501	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv34439	chr12:48541757-48779562	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	esv2757502	chr12:48547128-48779562	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv33956	chr12:48565643-48645561	Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6580661	ZNF641	cis	Muscle Skeletal	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48611800-48615400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:48612000-48629600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr12:48612200-48635600	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:48613000-48615600	Weak transcription	Primary monocytes fromperipheralblood	blood

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