Variant report

Variant	rs4650200
Chromosome Location	chr1:73652197-73652198
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10749816	0.84[ASN][1000 genomes]
rs10789358	0.84[ASN][1000 genomes]
rs10789359	0.87[ASN][1000 genomes]
rs10890011	0.84[ASN][1000 genomes]
rs10890012	0.86[ASN][1000 genomes]
rs10890013	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10890014	0.86[ASN][1000 genomes]
rs10890015	0.86[ASN][1000 genomes]
rs10890016	0.84[ASN][1000 genomes]
rs11210143	0.84[ASN][1000 genomes]
rs11210155	0.86[ASN][1000 genomes]
rs11210156	0.86[ASN][1000 genomes]
rs11210157	0.86[ASN][1000 genomes]
rs11210160	0.86[ASN][1000 genomes]
rs11210161	0.86[ASN][1000 genomes]
rs11210162	0.86[ASN][1000 genomes]
rs11210163	0.86[ASN][1000 genomes]
rs11210164	0.86[ASN][1000 genomes]
rs11210165	0.86[ASN][1000 genomes]
rs11210166	0.84[ASN][1000 genomes]
rs11210167	0.84[ASN][1000 genomes]
rs11210168	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11210170	0.84[ASN][1000 genomes]
rs11210172	0.87[ASN][1000 genomes]
rs11210174	0.85[ASN][1000 genomes]
rs11210180	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11582461	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11589897	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12034885	0.90[EUR][1000 genomes]
rs12037338	0.80[ASN][1000 genomes]
rs12059553	0.83[ASN][1000 genomes]
rs12087611	0.85[ASN][1000 genomes]
rs12122520	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12122901	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12124553	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12126688	0.85[ASN][1000 genomes]
rs12128855	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12133863	0.92[ASN][1000 genomes]
rs12133935	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12136496	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12137298	0.87[ASN][1000 genomes]
rs12137388	0.86[ASN][1000 genomes]
rs12143587	0.85[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12742692	0.84[ASN][1000 genomes]
rs1923240	0.96[CEU][hapmap]
rs34548060	0.86[ASN][1000 genomes]
rs34719239	0.86[ASN][1000 genomes]
rs34868208	0.86[ASN][1000 genomes]
rs34956095	0.86[ASN][1000 genomes]
rs35133930	0.85[ASN][1000 genomes]
rs35209284	0.86[ASN][1000 genomes]
rs35286654	0.85[ASN][1000 genomes]
rs35350320	0.87[ASN][1000 genomes]
rs35446706	0.86[ASN][1000 genomes]
rs35489458	0.86[ASN][1000 genomes]
rs35578487	0.86[ASN][1000 genomes]
rs36051652	0.86[ASN][1000 genomes]
rs36053729	0.86[ASN][1000 genomes]
rs4129350	0.86[EUR][1000 genomes]
rs4274014	0.92[EUR][1000 genomes]
rs4294371	0.86[ASN][1000 genomes]
rs4367754	0.86[ASN][1000 genomes]
rs4391625	0.84[ASN][1000 genomes]
rs4492565	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4503305	0.86[ASN][1000 genomes]
rs4537504	0.86[ASN][1000 genomes]
rs4578169	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4579710	0.86[ASN][1000 genomes]
rs4592219	0.86[ASN][1000 genomes]
rs4593762	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4601539	0.87[ASN][1000 genomes]
rs4607818	0.87[ASN][1000 genomes]
rs4641264	0.87[ASN][1000 genomes]
rs4649981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4650193	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4650194	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4650195	0.86[ASN][1000 genomes]
rs4650196	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4650197	0.86[ASN][1000 genomes]
rs4650199	0.93[EUR][1000 genomes]
rs61765598	0.86[ASN][1000 genomes]
rs6657881	0.85[ASN][1000 genomes]
rs6657885	0.85[ASN][1000 genomes]
rs6658012	0.86[ASN][1000 genomes]
rs6666765	0.86[ASN][1000 genomes]
rs6671028	0.86[ASN][1000 genomes]
rs6674333	0.86[ASN][1000 genomes]
rs6674404	0.86[ASN][1000 genomes]
rs6683380	0.86[ASN][1000 genomes]
rs6684331	0.86[ASN][1000 genomes]
rs6686255	0.86[ASN][1000 genomes]
rs6694634	0.86[ASN][1000 genomes]
rs6695455	0.86[ASN][1000 genomes]
rs6695460	0.86[ASN][1000 genomes]
rs6697098	0.86[ASN][1000 genomes]
rs6698500	0.86[ASN][1000 genomes]
rs6699861	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6700625	0.86[ASN][1000 genomes]
rs6703953	0.85[ASN][1000 genomes]
rs67437638	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7514409	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7545548	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005356	chr1:73542786-74124065	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv870774	chr1:73560811-73706449	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2757736	chr1:73613099-73775684	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2758942	chr1:73613099-73775684	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv870886	chr1:73634013-73790683	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
6	nsv870929	chr1:73644577-73776673	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
7	nsv870622	chr1:73647909-73776673	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
8	nsv871554	chr1:73647909-73882880	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv870536	chr1:73647909-74031554	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73642800-73653600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:73651400-73652800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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