Variant report

Variant	rs10017699
Chromosome Location	chr4:131020490-131020491
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10014736	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10025574	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10518562	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11933649	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11935280	0.84[AFR][1000 genomes]
rs12186167	0.91[ASN][1000 genomes]
rs13136824	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13147127	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13434533	0.88[ASN][1000 genomes]
rs17405853	0.84[AFR][1000 genomes]
rs17471046	0.88[AFR][1000 genomes]
rs2391597	0.91[ASN][1000 genomes]
rs28363914	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28374770	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28392536	0.86[ASN][1000 genomes]
rs28415658	0.91[AFR][1000 genomes]
rs28438639	0.88[ASN][1000 genomes]
rs28453003	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28465597	0.86[ASN][1000 genomes]
rs28548359	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28650462	0.83[ASN][1000 genomes]
rs35319540	0.88[AFR][1000 genomes]
rs35673533	0.81[AFR][1000 genomes]
rs55815336	0.86[ASN][1000 genomes]
rs59235089	0.86[ASN][1000 genomes]
rs6840686	0.90[ASN][1000 genomes]
rs71613297	0.85[ASN][1000 genomes]
rs71613299	0.84[AFR][1000 genomes]
rs949531	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs949532	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs958409	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv595414	chr4:130983055-131024471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv595415	chr4:130983605-131046911	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv595416	chr4:130998472-131834405	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762461	chr4:131004382-131391658	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131019600-131020800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr4:131019800-131020600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:131020000-131020800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:131020000-131021400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:131020200-131021000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:131020400-131021000	Enhancers	Brain Anterior Caudate	brain

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