Variant report

Variant	rs9342743
Chromosome Location	chr6:69859639-69859640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11759629	0.81[ASN][1000 genomes]
rs11759965	0.81[ASN][1000 genomes]
rs11968068	0.81[ASN][1000 genomes]
rs12527069	0.89[ASN][1000 genomes]
rs13214486	0.99[EUR][1000 genomes]
rs1482326	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1482328	0.81[ASN][1000 genomes]
rs1482329	0.81[ASN][1000 genomes]
rs1482331	0.81[ASN][1000 genomes]
rs1567659	0.81[ASN][1000 genomes]
rs1586042	0.89[ASN][1000 genomes]
rs1586043	0.89[ASN][1000 genomes]
rs1592054	0.89[ASN][1000 genomes]
rs1592056	0.89[ASN][1000 genomes]
rs1600873	0.89[ASN][1000 genomes]
rs1600876	0.81[EUR][1000 genomes]
rs17432036	0.81[ASN][1000 genomes]
rs17509972	0.81[ASN][1000 genomes]
rs17509993	0.81[ASN][1000 genomes]
rs1825195	0.81[ASN][1000 genomes]
rs1825196	0.89[ASN][1000 genomes]
rs2128291	0.89[ASN][1000 genomes]
rs2343257	0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2343259	1.00[EUR][1000 genomes]
rs2343261	0.99[EUR][1000 genomes]
rs3778238	0.81[ASN][1000 genomes]
rs4457127	0.89[ASN][1000 genomes]
rs4706866	0.81[ASN][1000 genomes]
rs55752088	0.89[ASN][1000 genomes]
rs56199922	0.89[ASN][1000 genomes]
rs62406787	0.81[ASN][1000 genomes]
rs62406790	0.93[ASN][1000 genomes]
rs62406791	0.81[ASN][1000 genomes]
rs62406797	0.89[ASN][1000 genomes]
rs6918978	0.81[ASN][1000 genomes]
rs6920644	0.81[ASN][1000 genomes]
rs6929969	0.89[ASN][1000 genomes]
rs7747753	0.89[ASN][1000 genomes]
rs7760630	0.81[ASN][1000 genomes]
rs9294820	0.81[ASN][1000 genomes]
rs9294821	0.81[ASN][1000 genomes]
rs9294822	0.81[ASN][1000 genomes]
rs9342742	0.81[ASN][1000 genomes]
rs9346266	0.89[ASN][1000 genomes]
rs9351745	0.81[ASN][1000 genomes]
rs9360375	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9360376	0.81[ASN][1000 genomes]
rs9360379	0.89[ASN][1000 genomes]
rs9446099	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886137	chr6:69684850-70095690	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv526130	chr6:69851816-69922327	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1029637	chr6:69855697-69916758	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69856400-69861600	Weak transcription	Fetal Brain Female	brain
2	chr6:69856400-69874000	Weak transcription	Brain Angular Gyrus	brain
3	chr6:69858200-69860400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr6:69859600-69860400	Strong transcription	Fetal Lung	lung

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