Variant report

Variant	rs817130
Chromosome Location	chr17:67342768-67342769
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1154017	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1222550	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1222599	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1642220	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1662694	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs182834	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2441360	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs333911	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs333912	0.93[EUR][1000 genomes]
rs333913	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs333914	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs333915	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs333916	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs333917	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs333918	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs333919	0.96[EUR][1000 genomes]
rs333920	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs333921	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs482524	0.82[AMR][1000 genomes]
rs489695	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs491516	0.89[EUR][1000 genomes]
rs506726	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs517988	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs518132	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs569063	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs575988	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs817129	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833527	chr17:67240575-67400871	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67339400-67355200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr17:67340000-67343000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr17:67341400-67342800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr17:67341400-67343000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr17:67342400-67343000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr17:67342400-67343000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr17:67342600-67343400	Enhancers	Skeletal Muscle Male	skeletal muscle

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