Variant report

Variant	rs9799801
Chromosome Location	chr4:86543614-86543615
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10000472	0.84[EUR][1000 genomes]
rs10017042	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10018069	0.84[EUR][1000 genomes]
rs10018180	0.84[EUR][1000 genomes]
rs10018546	0.83[EUR][1000 genomes]
rs10028585	0.84[EUR][1000 genomes]
rs1031988	0.84[EUR][1000 genomes]
rs10454245	0.84[EUR][1000 genomes]
rs12503598	0.84[EUR][1000 genomes]
rs12504294	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12506009	0.84[EUR][1000 genomes]
rs12506100	0.84[EUR][1000 genomes]
rs12506145	0.84[EUR][1000 genomes]
rs12640411	0.84[EUR][1000 genomes]
rs12641068	0.84[EUR][1000 genomes]
rs12644260	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12644694	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12644703	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12646241	0.83[EUR][1000 genomes]
rs12647949	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12648939	0.83[EUR][1000 genomes]
rs12650652	0.83[EUR][1000 genomes]
rs1384132	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1384134	0.84[EUR][1000 genomes]
rs1384135	0.84[EUR][1000 genomes]
rs1471605	0.84[EUR][1000 genomes]
rs1600840	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1905081	0.82[EUR][1000 genomes]
rs1905082	0.83[EUR][1000 genomes]
rs1905083	0.83[EUR][1000 genomes]
rs1905084	0.83[EUR][1000 genomes]
rs2086575	0.84[EUR][1000 genomes]
rs2128185	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28361935	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28423069	0.84[EUR][1000 genomes]
rs28475794	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28481407	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28483433	0.84[EUR][1000 genomes]
rs28537622	0.82[EUR][1000 genomes]
rs28565549	0.82[EUR][1000 genomes]
rs28591298	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs28719006	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28863335	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28867780	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28888099	0.85[EUR][1000 genomes]
rs2904073	0.81[EUR][1000 genomes]
rs35592449	0.84[EUR][1000 genomes]
rs4285081	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4286512	0.81[EUR][1000 genomes]
rs4447855	0.83[EUR][1000 genomes]
rs4450919	0.81[EUR][1000 genomes]
rs4693122	0.83[EUR][1000 genomes]
rs4693716	0.83[EUR][1000 genomes]
rs4693723	0.83[EUR][1000 genomes]
rs4693725	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4693726	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4693727	0.84[EUR][1000 genomes]
rs4693728	0.84[EUR][1000 genomes]
rs55798888	0.84[EUR][1000 genomes]
rs56266001	0.83[EUR][1000 genomes]
rs56853324	0.82[EUR][1000 genomes]
rs57572817	0.84[EUR][1000 genomes]
rs57626737	0.83[EUR][1000 genomes]
rs59051404	0.84[EUR][1000 genomes]
rs59682579	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59940085	0.83[EUR][1000 genomes]
rs60629877	0.83[EUR][1000 genomes]
rs61120164	0.84[EUR][1000 genomes]
rs61255139	0.83[EUR][1000 genomes]
rs61503855	0.83[EUR][1000 genomes]
rs62315277	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62315278	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62317184	0.83[EUR][1000 genomes]
rs62317186	0.84[EUR][1000 genomes]
rs62317188	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62317189	0.84[EUR][1000 genomes]
rs62317213	0.84[EUR][1000 genomes]
rs62317214	0.84[EUR][1000 genomes]
rs62317215	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62317218	0.84[EUR][1000 genomes]
rs6531846	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6531847	0.84[EUR][1000 genomes]
rs67431978	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6814977	0.83[EUR][1000 genomes]
rs6817114	0.84[EUR][1000 genomes]
rs6817221	0.84[EUR][1000 genomes]
rs6817542	0.84[EUR][1000 genomes]
rs6817549	0.84[EUR][1000 genomes]
rs72613144	0.83[EUR][1000 genomes]
rs7655020	0.84[EUR][1000 genomes]
rs7669207	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7669879	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7671404	0.83[EUR][1000 genomes]
rs7672353	0.83[EUR][1000 genomes]
rs7681072	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7689508	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7697937	0.84[EUR][1000 genomes]
rs7698610	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9799651	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9884932	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9996348	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9996446	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9997730	0.81[AMR][1000 genomes];0.84[EUR][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	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9799801	ARHGAP24	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86525600-86559200	Weak transcription	HSMM	muscle
2	chr4:86528400-86553600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:86537600-86549200	Weak transcription	Primary B cells from cord blood	blood
4	chr4:86538000-86547800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:86542400-86548800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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