Variant report

Variant	rs7297032
Chromosome Location	chr12:30317071-30317072
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:30307525..30310508-chr12:30315898..30318662,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10771639	0.92[EUR][1000 genomes]
rs10771640	0.93[EUR][1000 genomes]
rs10771641	0.86[EUR][1000 genomes]
rs10771642	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10771647	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10771648	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10843618	0.91[EUR][1000 genomes]
rs10843619	0.81[EUR][1000 genomes]
rs10843620	0.81[EUR][1000 genomes]
rs10843627	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11050670	0.80[EUR][1000 genomes]
rs11050672	0.91[EUR][1000 genomes]
rs11050674	0.80[EUR][1000 genomes]
rs11050675	0.81[EUR][1000 genomes]
rs12366875	0.81[EUR][1000 genomes]
rs12826253	0.81[EUR][1000 genomes]
rs1385562	0.80[EUR][1000 genomes]
rs1385563	0.81[EUR][1000 genomes]
rs1485425	0.93[EUR][1000 genomes]
rs1552342	0.81[EUR][1000 genomes]
rs1552343	0.81[EUR][1000 genomes]
rs1552344	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1909182	0.80[AMR][1000 genomes]
rs1909183	0.81[EUR][1000 genomes]
rs1973268	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2171038	0.81[EUR][1000 genomes]
rs2200410	0.81[EUR][1000 genomes]
rs2351209	0.93[EUR][1000 genomes]
rs2351210	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2351211	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4244851	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4930886	0.80[EUR][1000 genomes]
rs4930888	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4930889	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4930890	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4931271	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6487880	0.95[EUR][1000 genomes]
rs6487881	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6487883	0.85[EUR][1000 genomes]
rs72640154	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7296068	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7299613	0.81[EUR][1000 genomes]
rs7310880	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7311139	0.96[EUR][1000 genomes]
rs7313801	0.81[EUR][1000 genomes]
rs8181729	0.92[EUR][1000 genomes]
rs901075	0.93[EUR][1000 genomes]
rs901076	0.93[EUR][1000 genomes]
rs901077	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948495	chr12:30090771-30344772	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1042081	chr12:30147993-30344670	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv541436	chr12:30147993-30344670	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv821695	chr12:30287314-30450174	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1050757	chr12:30288879-30329142	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1035561	chr12:30288879-30336486	Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv516421	chr12:30309076-30411299	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7297032	CCDC91	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30316600-30317200	Weak transcription	HSMMtube	muscle
2	chr12:30316800-30319200	Enhancers	Fetal Lung	lung

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