Variant report

Variant	rs263249
Chromosome Location	chr8:131795260-131795261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10097218	0.81[ASN][1000 genomes]
rs10435556	0.83[ASN][1000 genomes]
rs10435557	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956547	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956548	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956551	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956552	0.81[ASN][1000 genomes]
rs10956553	0.80[ASN][1000 genomes]
rs11984653	0.81[ASN][1000 genomes]
rs11993878	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12545452	0.80[ASN][1000 genomes]
rs12545966	0.80[ASN][1000 genomes]
rs12546136	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12550841	0.81[ASN][1000 genomes]
rs13250130	0.81[ASN][1000 genomes]
rs13258564	0.81[ASN][1000 genomes]
rs13259683	0.81[ASN][1000 genomes]
rs13278937	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1509854	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509855	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509856	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509857	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509858	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509859	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1509860	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17225213	0.81[ASN][1000 genomes]
rs17226139	0.80[ASN][1000 genomes]
rs17316525	0.81[ASN][1000 genomes]
rs182026	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1836628	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1848776	0.83[ASN][1000 genomes]
rs1848777	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2164304	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2196315	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2572867	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs263231	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs263245	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs263247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2889477	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs368403	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3793387	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4339660	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5000695	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6470852	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6997501	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6998308	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7002481	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7007094	0.83[ASN][1000 genomes]
rs7010990	0.83[ASN][1000 genomes]
rs7014884	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7015398	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs873666	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs873667	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9297815	0.81[ASN][1000 genomes]
rs9649965	0.80[ASN][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	nsv612294	chr8:131645079-131923377	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv891448	chr8:131668278-131968469	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv831462	chr8:131704119-131895793	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1034107	chr8:131740146-131985765	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539747	chr8:131740146-131985765	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3344408	chr8:131794170-131798768	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131789600-131814800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:131790000-131813800	Weak transcription	Brain Substantia Nigra	brain
3	chr8:131791600-131814000	Weak transcription	Brain Angular Gyrus	brain
4	chr8:131792400-131797200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr8:131792400-131798400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:131794600-131799800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:131795000-131801800	Weak transcription	Brain Anterior Caudate	brain
8	chr8:131795200-131796000	Enhancers	Spleen	Spleen
9	chr8:131795200-131796200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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