Variant report

Variant	rs10163840
Chromosome Location	chr18:39162137-39162138
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10163854	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10502769	0.83[ASN][1000 genomes]
rs10502770	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10502771	1.00[ASN][1000 genomes]
rs10502772	0.82[EUR][1000 genomes]
rs16974995	0.83[ASN][1000 genomes]
rs16974999	0.83[ASN][1000 genomes]
rs16975000	0.81[EUR][1000 genomes]
rs16975004	0.81[EUR][1000 genomes]
rs16975007	0.81[EUR][1000 genomes]
rs16975010	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975012	0.81[EUR][1000 genomes]
rs16975017	0.81[EUR][1000 genomes]
rs16975021	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975022	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16975025	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1942063	1.00[ASN][1000 genomes]
rs1942069	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1942070	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28374486	0.81[EUR][1000 genomes]
rs28414473	0.81[EUR][1000 genomes]
rs35462279	0.81[EUR][1000 genomes]
rs4404160	0.81[EUR][1000 genomes]
rs55797333	1.00[ASN][1000 genomes]
rs56341064	0.83[ASN][1000 genomes]
rs56812327	1.00[ASN][1000 genomes]
rs57249168	1.00[ASN][1000 genomes]
rs58350157	0.81[EUR][1000 genomes]
rs6507425	0.82[EUR][1000 genomes]
rs7229356	0.81[EUR][1000 genomes]
rs7244165	0.81[EUR][1000 genomes]
rs72905919	0.83[EUR][1000 genomes]
rs72905923	0.81[EUR][1000 genomes]
rs72905924	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72905927	0.83[EUR][1000 genomes]
rs72905935	0.83[EUR][1000 genomes]
rs72905937	0.83[EUR][1000 genomes]
rs72905948	0.81[EUR][1000 genomes]
rs72905963	1.00[ASN][1000 genomes]
rs72905965	1.00[ASN][1000 genomes]
rs72905967	1.00[ASN][1000 genomes]
rs72905973	0.81[EUR][1000 genomes]
rs72905979	1.00[ASN][1000 genomes]
rs72905981	0.81[EUR][1000 genomes]
rs72905986	0.81[EUR][1000 genomes]
rs72905989	0.81[EUR][1000 genomes]
rs72907804	0.81[EUR][1000 genomes]
rs72907808	0.81[EUR][1000 genomes]
rs72907815	0.81[EUR][1000 genomes]
rs72907817	0.81[EUR][1000 genomes]
rs72907819	0.81[EUR][1000 genomes]
rs72907821	0.81[EUR][1000 genomes]
rs72907830	0.81[EUR][1000 genomes]
rs72907836	0.81[EUR][1000 genomes]
rs72907842	0.81[EUR][1000 genomes]
rs72907845	0.81[EUR][1000 genomes]
rs72907847	0.81[EUR][1000 genomes]
rs72907850	0.81[EUR][1000 genomes]
rs72907851	0.81[EUR][1000 genomes]
rs72907855	0.81[EUR][1000 genomes]
rs8098315	0.81[EUR][1000 genomes]
rs8098394	0.81[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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39160800-39167600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr18:39160800-39168400	Weak transcription	Fetal Heart	heart
3	chr18:39161000-39168600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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