Variant report

Variant	rs9643785
Chromosome Location	chr8:52574106-52574107
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10106091	0.80[EUR][1000 genomes]
rs10958291	0.88[ASN][1000 genomes]
rs10958293	0.94[ASN][1000 genomes]
rs10958294	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10958296	0.80[EUR][1000 genomes]
rs11781376	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11782339	0.92[ASN][1000 genomes]
rs12548130	0.94[ASN][1000 genomes]
rs12677123	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13251959	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13265125	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13268396	0.87[EUR][1000 genomes]
rs13268711	0.87[EUR][1000 genomes]
rs13274101	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13277004	0.81[EUR][1000 genomes]
rs13279418	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16916673	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16916741	0.81[EUR][1000 genomes]
rs16916756	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28492012	0.86[ASN][1000 genomes]
rs34228216	0.86[EUR][1000 genomes]
rs34276635	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35153909	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35365537	0.82[EUR][1000 genomes]
rs36070314	0.87[ASN][1000 genomes]
rs36075262	0.80[EUR][1000 genomes]
rs4275221	0.87[EUR][1000 genomes]
rs4291264	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4400372	0.80[EUR][1000 genomes]
rs4469447	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4873199	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4873568	0.94[ASN][1000 genomes]
rs4873572	0.81[EUR][1000 genomes]
rs4873573	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6981117	0.94[ASN][1000 genomes]
rs6981260	0.80[EUR][1000 genomes]
rs6981313	0.94[ASN][1000 genomes]
rs6986571	0.80[EUR][1000 genomes]
rs6986605	0.80[EUR][1000 genomes]
rs6987346	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6995555	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6999693	0.80[EUR][1000 genomes]
rs7000785	0.94[ASN][1000 genomes]
rs7007297	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7007671	0.81[EUR][1000 genomes]
rs7823666	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7836565	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7845169	0.88[ASN][1000 genomes]
rs9650178	0.94[ASN][1000 genomes]
rs9650303	0.89[EUR][1000 genomes];0.86[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	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv890895	chr8:52190571-52615191	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1018429	chr8:52411443-52878946	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1034856	chr8:52411443-52886765	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv831313	chr8:52458835-52638968	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52566400-52580800	Weak transcription	Aorta	Aorta
2	chr8:52566800-52575200	Weak transcription	Fetal Lung	lung
3	chr8:52566800-52577400	Weak transcription	Psoas Muscle	Psoas
4	chr8:52568200-52577000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr8:52568600-52576000	Weak transcription	Fetal Heart	heart
6	chr8:52570800-52575600	Weak transcription	Left Ventricle	heart
7	chr8:52573200-52574400	Enhancers	Right Ventricle	heart
8	chr8:52573400-52574400	Enhancers	Right Atrium	heart
9	chr8:52574000-52574400	Enhancers	Fetal Muscle Leg	muscle

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