Variant report

Variant	rs9418311
Chromosome Location	chr10:38269711-38269712
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	chr10:38265631..38267424-chr10:38268939..38270745,3	K562	blood:
2	chr10:38265225..38267424-chr10:38268939..38271746,5	K562	blood:

Variant related genes	Relation type
ENSG00000226447	Chromatin interaction
ENSG00000175395	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1208578	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1208619	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1208621	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12243792	0.80[EUR][1000 genomes]
rs12412402	0.80[EUR][1000 genomes]
rs12413083	0.94[ASN][1000 genomes]
rs12414618	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1735625	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17608725	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs176831	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs176832	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1779073	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs200907	0.86[EUR][1000 genomes]
rs200909	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs200913	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs200914	0.84[EUR][1000 genomes]
rs200941	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2021651	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2178958	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2293962	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2472153	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2472159	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2472160	0.86[ASN][1000 genomes]
rs2474542	0.84[ASN][1000 genomes]
rs2474545	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2474553	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2480521	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2489166	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2504137	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2505218	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2738221	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2753883	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs55742761	0.81[EUR][1000 genomes]
rs59486180	0.81[EUR][1000 genomes]
rs766362	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7895468	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][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	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv1051121	chr10:38155991-38426204	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv540565	chr10:38155991-38426204	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv534122	chr10:38240258-38356008	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9418311	ZNF37A	Cis_1M	lymphoblastoid	RTeQTL
rs9418311	HSD17B7///HSD17B7P2///LOC730412	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38266000-38271600	Weak transcription	HSMMtube	muscle

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