Variant report

Variant	rs41930
Chromosome Location	chr7:117933479-117933480
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:117914543..117916311-chr7:117931955..117934025,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10247768	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10487392	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11542074	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11974039	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs11983651	0.82[EUR][1000 genomes]
rs12154684	0.84[EUR][1000 genomes]
rs1544583	0.81[EUR][1000 genomes]
rs1544584	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17140984	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17141053	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2215628	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2286863	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28260	0.89[EUR][1000 genomes]
rs33924981	0.85[EUR][1000 genomes]
rs34010516	0.80[EUR][1000 genomes]
rs34019303	0.85[EUR][1000 genomes]
rs35218902	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35485182	0.84[EUR][1000 genomes]
rs41903	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs41904	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs41912	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41921	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41923	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41924	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41925	0.89[EUR][1000 genomes]
rs41931	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs41936	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41962	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41989	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4260839	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs45604739	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4730837	0.85[EUR][1000 genomes]
rs4730868	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62466471	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62466515	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62468297	0.83[EUR][1000 genomes]
rs62469806	0.81[EUR][1000 genomes]
rs6960940	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7786233	0.84[EUR][1000 genomes]
rs7801976	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7811687	0.85[EUR][1000 genomes]
rs9641593	0.81[AMR][1000 genomes];0.85[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	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	nsv889090	chr7:117865940-118067460	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv889091	chr7:117899190-117963926	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1029103	chr7:117917362-118035987	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2764014	chr7:117917374-118035999	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv608261	chr7:117917719-117965390	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv608262	chr7:117926753-118036133	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs41930	LSM8	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117933400-117933800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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