Variant report

Variant	rs1383272
Chromosome Location	chr8:50165832-50165833
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10092709	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10097641	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1021036	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10504077	0.89[EUR][1000 genomes]
rs10808750	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10957382	0.81[AFR][1000 genomes]
rs10957383	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10957385	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11777050	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11986211	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11998708	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13263230	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1383279	0.81[AFR][1000 genomes]
rs1842400	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2219896	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2385328	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2385330	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2385331	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35395861	0.90[EUR][1000 genomes]
rs4256605	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4461912	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4501593	0.90[EUR][1000 genomes]
rs4873325	0.81[EUR][1000 genomes]
rs4873347	0.85[EUR][1000 genomes]
rs4873348	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4873349	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55987135	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62508747	0.90[EUR][1000 genomes]
rs6472291	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6982179	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6988643	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6999524	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7006071	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7012516	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7818564	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7824009	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7828104	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7833419	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7836969	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7840704	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7841358	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7844505	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7845374	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025068	chr8:49953397-50370208	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1034908	chr8:50023423-50416049	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv539601	chr8:50023423-50416049	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1024410	chr8:50037085-50511501	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv428517	chr8:50094920-50232993	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv890855	chr8:50109365-50252962	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv890856	chr8:50133485-50272497	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv890857	chr8:50133485-50469764	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50163400-50166000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:50165000-50169800	Weak transcription	Fetal Intestine Small	intestine
3	chr8:50165400-50170000	Weak transcription	Stomach Mucosa	stomach
4	chr8:50165600-50169800	Weak transcription	Fetal Intestine Large	intestine
5	chr8:50165600-50170400	Weak transcription	K562	blood

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