Variant report

Variant	rs4259055
Chromosome Location	chr4:86582889-86582890
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10000472	0.90[EUR][1000 genomes]
rs10017042	0.89[EUR][1000 genomes]
rs10018069	0.90[EUR][1000 genomes]
rs10018180	0.90[EUR][1000 genomes]
rs10018546	0.90[EUR][1000 genomes]
rs10028585	0.90[EUR][1000 genomes]
rs1031988	0.90[EUR][1000 genomes]
rs10454245	0.88[EUR][1000 genomes]
rs11097066	0.86[EUR][1000 genomes]
rs12503598	0.90[EUR][1000 genomes]
rs12504294	0.88[EUR][1000 genomes]
rs12506009	0.90[EUR][1000 genomes]
rs12506100	0.90[EUR][1000 genomes]
rs12506145	0.90[EUR][1000 genomes]
rs12506596	0.85[EUR][1000 genomes]
rs12640411	0.90[EUR][1000 genomes]
rs12641068	0.89[EUR][1000 genomes]
rs12644260	0.91[EUR][1000 genomes]
rs12644694	0.91[EUR][1000 genomes]
rs12644703	0.91[EUR][1000 genomes]
rs12646241	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12647949	0.88[EUR][1000 genomes]
rs12648939	0.91[EUR][1000 genomes]
rs12650652	0.91[EUR][1000 genomes]
rs1384132	0.89[EUR][1000 genomes]
rs1384134	0.90[EUR][1000 genomes]
rs1384135	0.90[EUR][1000 genomes]
rs1471605	0.90[EUR][1000 genomes]
rs1471607	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1600840	0.89[EUR][1000 genomes]
rs17389300	0.85[EUR][1000 genomes]
rs17389342	0.85[EUR][1000 genomes]
rs1905081	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1905082	0.91[EUR][1000 genomes]
rs1905083	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1905084	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2086575	0.88[EUR][1000 genomes]
rs2128185	0.90[EUR][1000 genomes]
rs28361935	0.90[EUR][1000 genomes]
rs28423069	0.90[EUR][1000 genomes]
rs28454938	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28475794	0.91[EUR][1000 genomes]
rs28481407	0.88[EUR][1000 genomes]
rs28483433	0.90[EUR][1000 genomes]
rs28537622	0.90[EUR][1000 genomes]
rs28565549	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28591298	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2869363	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28719006	0.89[EUR][1000 genomes]
rs28863335	0.88[EUR][1000 genomes]
rs28867780	0.88[EUR][1000 genomes]
rs28888099	0.88[EUR][1000 genomes]
rs2904073	0.87[EUR][1000 genomes]
rs34837792	0.89[EUR][1000 genomes]
rs35592449	0.88[EUR][1000 genomes]
rs4285081	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4286512	0.92[EUR][1000 genomes]
rs4447855	0.91[EUR][1000 genomes]
rs4450919	0.87[EUR][1000 genomes]
rs4693122	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4693124	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4693716	0.89[EUR][1000 genomes]
rs4693723	0.87[EUR][1000 genomes]
rs4693725	0.87[EUR][1000 genomes]
rs4693726	0.87[EUR][1000 genomes]
rs4693727	0.90[EUR][1000 genomes]
rs4693728	0.90[EUR][1000 genomes]
rs55798888	0.90[EUR][1000 genomes]
rs56266001	0.88[EUR][1000 genomes]
rs56853324	0.87[EUR][1000 genomes]
rs57572817	0.88[EUR][1000 genomes]
rs57626737	0.88[EUR][1000 genomes]
rs59051404	0.90[EUR][1000 genomes]
rs59682579	0.88[EUR][1000 genomes]
rs59940085	0.89[EUR][1000 genomes]
rs60629877	0.88[EUR][1000 genomes]
rs61120164	0.90[EUR][1000 genomes]
rs61255139	0.89[EUR][1000 genomes]
rs61503855	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61660116	0.85[EUR][1000 genomes]
rs62315277	0.91[EUR][1000 genomes]
rs62315278	0.91[EUR][1000 genomes]
rs62315287	0.89[EUR][1000 genomes]
rs62315290	0.89[EUR][1000 genomes]
rs62317179	0.85[EUR][1000 genomes]
rs62317184	0.89[EUR][1000 genomes]
rs62317186	0.88[EUR][1000 genomes]
rs62317188	0.88[EUR][1000 genomes]
rs62317189	0.88[EUR][1000 genomes]
rs62317213	0.90[EUR][1000 genomes]
rs62317214	0.90[EUR][1000 genomes]
rs62317215	0.90[EUR][1000 genomes]
rs62317218	0.90[EUR][1000 genomes]
rs6531846	0.90[EUR][1000 genomes]
rs6531847	0.90[EUR][1000 genomes]
rs67431978	0.90[EUR][1000 genomes]
rs6814977	0.89[EUR][1000 genomes]
rs6817114	0.90[EUR][1000 genomes]
rs6817221	0.90[EUR][1000 genomes]
rs6817542	0.90[EUR][1000 genomes]
rs6817549	0.90[EUR][1000 genomes]
rs72613143	0.85[EUR][1000 genomes]
rs72613144	0.89[EUR][1000 genomes]
rs7655020	0.90[EUR][1000 genomes]
rs7668677	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7669207	0.90[EUR][1000 genomes]
rs7669879	0.90[EUR][1000 genomes]
rs7671404	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7672353	0.91[EUR][1000 genomes]
rs7681072	0.88[EUR][1000 genomes]
rs7689508	0.89[EUR][1000 genomes]
rs7695028	0.83[EUR][1000 genomes]
rs7697937	0.89[EUR][1000 genomes]
rs7698610	0.88[EUR][1000 genomes]
rs9799651	0.88[EUR][1000 genomes]
rs9884932	0.89[EUR][1000 genomes]
rs9996348	0.88[EUR][1000 genomes]
rs9996446	0.88[EUR][1000 genomes]
rs9997730	0.90[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
rs4259055	ARHGAP24	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86570200-86593600	Weak transcription	HSMM	muscle
2	chr4:86580400-86593000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:86582400-86583400	Enhancers	Primary B cells from peripheral blood	blood
4	chr4:86582400-86590000	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr4:86582600-86589200	Weak transcription	Primary B cells from cord blood	blood
6	chr4:86582600-86589600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr4:86582600-86590200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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