Variant report

Variant	rs36018030
Chromosome Location	chr7:145881491-145881492
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	chr7:145879679..145882297-chr7:145885152..145887234,2	K562	blood:
2	chr7:145872793..145874958-chr7:145879839..145881542,2	K562	blood:

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10230226	0.97[ASN][1000 genomes]
rs10237336	0.97[ASN][1000 genomes]
rs10268545	0.97[ASN][1000 genomes]
rs10277217	0.93[ASN][1000 genomes]
rs11520906	1.00[ASN][1000 genomes]
rs11974152	0.97[ASN][1000 genomes]
rs11978140	0.97[ASN][1000 genomes]
rs11980028	0.97[ASN][1000 genomes]
rs12703770	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12703779	0.93[ASN][1000 genomes]
rs12703780	0.97[ASN][1000 genomes]
rs12703781	0.97[ASN][1000 genomes]
rs12703784	0.97[ASN][1000 genomes]
rs12703785	0.97[ASN][1000 genomes]
rs12703786	0.97[ASN][1000 genomes]
rs12703788	0.97[ASN][1000 genomes]
rs12703790	0.97[ASN][1000 genomes]
rs12703791	0.97[ASN][1000 genomes]
rs13221011	0.97[ASN][1000 genomes]
rs13223353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223500	0.93[ASN][1000 genomes]
rs13223589	0.93[ASN][1000 genomes]
rs13224076	0.97[ASN][1000 genomes]
rs13224183	0.97[ASN][1000 genomes]
rs13224771	1.00[ASN][1000 genomes]
rs13238577	0.97[ASN][1000 genomes]
rs13239694	1.00[ASN][1000 genomes]
rs13241192	0.97[ASN][1000 genomes]
rs13242084	1.00[ASN][1000 genomes]
rs13242684	0.93[ASN][1000 genomes]
rs13245661	1.00[ASN][1000 genomes]
rs1464959	0.97[ASN][1000 genomes]
rs1464960	0.97[ASN][1000 genomes]
rs1464961	0.97[ASN][1000 genomes]
rs1526079	1.00[ASN][1000 genomes]
rs17169989	1.00[ASN][1000 genomes]
rs17169990	1.00[ASN][1000 genomes]
rs17577839	1.00[ASN][1000 genomes]
rs1917936	0.93[ASN][1000 genomes]
rs2014200	0.97[ASN][1000 genomes]
rs2080179	0.97[ASN][1000 genomes]
rs2080180	0.97[ASN][1000 genomes]
rs2098288	0.97[ASN][1000 genomes]
rs2140950	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2430324	0.97[ASN][1000 genomes]
rs2430328	0.90[ASN][1000 genomes]
rs2462829	0.82[ASN][1000 genomes]
rs2462830	0.97[ASN][1000 genomes]
rs2539738	0.97[ASN][1000 genomes]
rs2539739	0.97[ASN][1000 genomes]
rs2539740	0.97[ASN][1000 genomes]
rs2539744	0.97[ASN][1000 genomes]
rs2539745	0.97[ASN][1000 genomes]
rs2539746	0.97[ASN][1000 genomes]
rs2539747	0.97[ASN][1000 genomes]
rs2693306	0.97[ASN][1000 genomes]
rs2693307	0.97[ASN][1000 genomes]
rs28600774	0.97[ASN][1000 genomes]
rs34053851	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34276665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34280066	0.96[EUR][1000 genomes]
rs34332205	1.00[ASN][1000 genomes]
rs35018596	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35273012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35491208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4327781	0.97[ASN][1000 genomes]
rs4345482	0.97[ASN][1000 genomes]
rs4445149	0.97[ASN][1000 genomes]
rs6464733	0.97[ASN][1000 genomes]
rs6464734	0.90[ASN][1000 genomes]
rs6464737	0.90[ASN][1000 genomes]
rs6464738	0.97[ASN][1000 genomes]
rs6464739	0.97[ASN][1000 genomes]
rs67123143	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67518892	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs67548137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68099112	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6946245	0.97[ASN][1000 genomes]
rs6947847	0.85[ASN][1000 genomes]
rs6959235	0.97[ASN][1000 genomes]
rs6960368	0.97[ASN][1000 genomes]
rs6960388	0.97[ASN][1000 genomes]
rs6960982	0.97[ASN][1000 genomes]
rs73160680	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7777761	0.97[ASN][1000 genomes]
rs7779760	0.97[ASN][1000 genomes]
rs7780228	0.97[ASN][1000 genomes]
rs7785592	0.97[ASN][1000 genomes]
rs7785673	0.93[ASN][1000 genomes]
rs7786007	0.97[ASN][1000 genomes]
rs7787269	0.97[ASN][1000 genomes]
rs7788768	0.90[ASN][1000 genomes]
rs7789370	0.97[ASN][1000 genomes]
rs7793060	0.97[ASN][1000 genomes]
rs7794609	0.97[ASN][1000 genomes]
rs7794731	0.97[ASN][1000 genomes]
rs7795190	0.93[ASN][1000 genomes]
rs7795488	0.97[ASN][1000 genomes]
rs7798919	0.97[ASN][1000 genomes]
rs7811486	0.97[ASN][1000 genomes]
rs802530	0.97[ASN][1000 genomes]
rs802532	0.97[ASN][1000 genomes]
rs802534	0.97[ASN][1000 genomes]
rs802535	0.97[ASN][1000 genomes]
rs802538	0.97[ASN][1000 genomes]
rs802539	0.97[ASN][1000 genomes]
rs802542	0.97[ASN][1000 genomes]
rs802543	0.97[ASN][1000 genomes]
rs802544	0.97[ASN][1000 genomes]
rs802546	0.97[ASN][1000 genomes]
rs802547	0.97[ASN][1000 genomes]
rs802548	0.97[ASN][1000 genomes]
rs802550	0.97[ASN][1000 genomes]
rs802552	0.97[ASN][1000 genomes]
rs802577	0.97[ASN][1000 genomes]
rs802580	0.97[ASN][1000 genomes]
rs802581	0.93[ASN][1000 genomes]
rs810596	0.97[ASN][1000 genomes]
rs940932	0.93[ASN][1000 genomes]
rs940933	0.87[ASN][1000 genomes]
rs955107	0.97[ASN][1000 genomes]
rs955108	0.97[ASN][1000 genomes]
rs959411	0.80[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	nsv889384	chr7:145541783-146239545	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1023861	chr7:145606069-145910049	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv539170	chr7:145606069-145910049	Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1020950	chr7:145683419-146264304	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv981604	chr7:145773003-145935052	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv608927	chr7:145803095-145882001	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv889386	chr7:145845418-145935428	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145874600-145887400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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