Variant report

Variant	rs7018436
Chromosome Location	chr8:10574848-10574849
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10572945..10574994-chr8:10579706..10582412,2	K562	blood:
2	chr8:10573494..10575019-chr8:10578805..10581206,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11993807	0.91[ASN][1000 genomes]
rs12544976	0.91[ASN][1000 genomes]
rs12547475	0.90[ASN][1000 genomes]
rs12547478	0.89[ASN][1000 genomes]
rs12679869	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13259730	0.93[ASN][1000 genomes]
rs13271462	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13277080	0.90[ASN][1000 genomes]
rs13278953	0.91[ASN][1000 genomes]
rs4321966	0.86[ASN][1000 genomes]
rs4484649	0.80[ASN][1000 genomes]
rs4489291	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4493874	0.94[ASN][1000 genomes]
rs6996979	0.88[ASN][1000 genomes]
rs6998295	0.86[ASN][1000 genomes]
rs7009586	0.94[ASN][1000 genomes]
rs7815363	0.88[ASN][1000 genomes]
rs7834573	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7844805	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1015932	chr8:10357101-10597856	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1021048	chr8:10504395-10591896	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
6	nsv527184	chr8:10530037-10589913	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1028266	chr8:10537081-10586112	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv1034829	chr8:10537081-10591896	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1032725	chr8:10561962-10585683	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1022582	chr8:10571218-10636162	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv539468	chr8:10571218-10636162	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10570200-10575000	Enhancers	Duodenum Mucosa	Duodenum
2	chr8:10570800-10575800	Enhancers	Lung	lung
3	chr8:10572000-10583000	Weak transcription	Liver	Liver
4	chr8:10572200-10575400	Enhancers	HUVEC	blood vessel
5	chr8:10572800-10575600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr8:10573200-10575600	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr8:10573400-10575200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:10573600-10575000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
9	chr8:10573600-10575600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:10573800-10575600	Enhancers	Left Ventricle	heart
11	chr8:10574000-10575000	Enhancers	Primary B cells from cord blood	blood
12	chr8:10574200-10575000	Enhancers	Adipose Nuclei	Adipose
13	chr8:10574200-10575200	Enhancers	Spleen	Spleen
14	chr8:10574200-10575800	Enhancers	Placenta	Placenta
15	chr8:10574200-10579400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:10574200-10579600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:10574200-10579600	Weak transcription	NHEK	skin
18	chr8:10574400-10575400	Enhancers	Primary B cells from peripheral blood	blood
19	chr8:10574400-10575400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
20	chr8:10574400-10575600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr8:10574400-10579600	Weak transcription	Esophagus	oesophagus
22	chr8:10574400-10579800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:10574600-10575000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
24	chr8:10574600-10575600	Enhancers	Right Atrium	heart
25	chr8:10574800-10575000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
26	chr8:10574800-10584200	Weak transcription	Hela-S3	cervix

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