Variant report

Variant	rs16975004
Chromosome Location	chr18:39160403-39160404
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10163840	0.81[EUR][1000 genomes]
rs10163854	0.93[EUR][1000 genomes]
rs10221329	0.80[EUR][1000 genomes]
rs10502770	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10502771	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10502772	0.89[EUR][1000 genomes]
rs11875076	0.85[EUR][1000 genomes]
rs13381575	0.98[EUR][1000 genomes]
rs13381786	1.00[CHB][hapmap]
rs1368833	0.93[EUR][1000 genomes]
rs1433929	0.93[EUR][1000 genomes]
rs1560844	0.96[EUR][1000 genomes]
rs16975000	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16975006	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs16975007	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975010	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16975012	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975017	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975020	1.00[ASN][1000 genomes]
rs16975021	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16975022	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16975025	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16975035	0.81[EUR][1000 genomes]
rs16975049	0.98[EUR][1000 genomes]
rs16975051	0.83[EUR][1000 genomes]
rs1942063	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1942065	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1942069	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1942070	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2156006	0.98[EUR][1000 genomes]
rs2315174	0.98[EUR][1000 genomes]
rs28374486	0.88[EUR][1000 genomes]
rs28414473	0.88[EUR][1000 genomes]
rs35462279	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4404160	0.88[EUR][1000 genomes]
rs55797333	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56812327	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57249168	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58350157	0.95[EUR][1000 genomes]
rs60047677	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6507424	0.96[EUR][1000 genomes]
rs6507425	0.89[EUR][1000 genomes]
rs6507428	0.93[EUR][1000 genomes]
rs7229356	0.88[EUR][1000 genomes]
rs7229794	0.83[AMR][1000 genomes]
rs7237488	0.93[EUR][1000 genomes]
rs7244165	0.88[EUR][1000 genomes]
rs72903987	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72903996	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72905903	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72905904	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72905906	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72905911	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72905915	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72905919	0.90[EUR][1000 genomes]
rs72905923	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905924	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72905927	0.90[EUR][1000 genomes]
rs72905935	0.90[EUR][1000 genomes]
rs72905937	0.90[EUR][1000 genomes]
rs72905948	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72905963	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72905965	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72905967	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72905973	0.88[EUR][1000 genomes]
rs72905979	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72905981	0.88[EUR][1000 genomes]
rs72905986	0.88[EUR][1000 genomes]
rs72905989	0.88[EUR][1000 genomes]
rs72907804	0.88[EUR][1000 genomes]
rs72907808	0.88[EUR][1000 genomes]
rs72907815	0.88[EUR][1000 genomes]
rs72907817	0.88[EUR][1000 genomes]
rs72907819	0.88[EUR][1000 genomes]
rs72907821	0.88[EUR][1000 genomes]
rs72907830	0.88[EUR][1000 genomes]
rs72907836	0.88[EUR][1000 genomes]
rs72907842	0.88[EUR][1000 genomes]
rs72907845	0.88[EUR][1000 genomes]
rs72907847	0.88[EUR][1000 genomes]
rs72907848	0.96[EUR][1000 genomes]
rs72907850	0.88[EUR][1000 genomes]
rs72907851	0.88[EUR][1000 genomes]
rs72907854	0.85[EUR][1000 genomes]
rs72907855	0.88[EUR][1000 genomes]
rs72907861	0.87[EUR][1000 genomes]
rs72907862	0.87[EUR][1000 genomes]
rs72909913	0.87[EUR][1000 genomes]
rs72909936	0.87[EUR][1000 genomes]
rs72909959	0.87[EUR][1000 genomes]
rs734357	0.98[EUR][1000 genomes]
rs73450796	0.98[EUR][1000 genomes]
rs8087434	0.96[EUR][1000 genomes]
rs8087485	0.98[EUR][1000 genomes]
rs8098315	0.88[EUR][1000 genomes]
rs8098394	0.88[EUR][1000 genomes]
rs9304250	0.83[EUR][1000 genomes]
rs9949338	0.93[EUR][1000 genomes]
rs9956251	0.95[EUR][1000 genomes]
rs9965809	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909564	chr18:38739067-39179256	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv2267	chr18:39123940-39169583	Enhancers Weak transcription Strong transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases
5	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39150400-39161400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr18:39158200-39160600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr18:39159400-39160800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr18:39159400-39160800	Enhancers	Fetal Heart	heart
5	chr18:39160400-39161000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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