Variant report

Variant	rs73691574
Chromosome Location	chr8:67661759-67661760
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11988681	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11991125	1.00[AMR][1000 genomes]
rs11992829	1.00[AMR][1000 genomes]
rs35063782	0.91[AFR][1000 genomes]
rs56856536	0.91[AFR][1000 genomes]
rs58411534	0.85[AFR][1000 genomes]
rs60017659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60434307	0.91[AFR][1000 genomes]
rs6991442	0.82[AFR][1000 genomes]
rs6992429	0.82[AFR][1000 genomes]
rs7001796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7001886	0.85[AFR][1000 genomes]
rs7003330	0.91[AFR][1000 genomes]
rs73691570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691576	1.00[AMR][1000 genomes]
rs73691581	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691596	0.94[AFR][1000 genomes]
rs73691602	0.91[AFR][1000 genomes]
rs73693607	0.85[AFR][1000 genomes]
rs73693608	0.91[AFR][1000 genomes]
rs73693609	0.91[AFR][1000 genomes]
rs73693616	0.85[AFR][1000 genomes]
rs73693617	0.85[AFR][1000 genomes]
rs73693618	0.85[AFR][1000 genomes]
rs9694590	0.91[AFR][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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv831346	chr8:67486555-67675324	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv1026746	chr8:67639626-67794164	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67626200-67664400	Weak transcription	Ovary	ovary
2	chr8:67626200-67665200	Weak transcription	Fetal Stomach	stomach
3	chr8:67627200-67665600	Weak transcription	Left Ventricle	heart
4	chr8:67632600-67662400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr8:67639600-67664400	Weak transcription	Thymus	Thymus
6	chr8:67641200-67666200	Weak transcription	Pancreas	Pancrea
7	chr8:67647800-67671000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:67651400-67663000	Weak transcription	Adipose Nuclei	Adipose
9	chr8:67651600-67664200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr8:67652200-67672400	Weak transcription	Fetal Intestine Small	intestine
11	chr8:67652400-67664200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:67652600-67664000	Weak transcription	Primary B cells from cord blood	blood
13	chr8:67656400-67679000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:67656600-67670400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:67657000-67662800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr8:67658400-67663000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr8:67658400-67663400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:67658800-67662400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:67658800-67663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:67660600-67661800	Enhancers	HSMMtube	muscle
21	chr8:67660800-67661800	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr8:67660800-67667800	Weak transcription	Brain Angular Gyrus	brain
23	chr8:67661000-67662200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:67661000-67664000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:67661000-67664200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr8:67661000-67664400	Weak transcription	Brain Anterior Caudate	brain
27	chr8:67661000-67664400	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr8:67661000-67668000	Weak transcription	Brain Substantia Nigra	brain
29	chr8:67661000-67673400	Weak transcription	Brain Hippocampus Middle	brain
30	chr8:67661200-67664200	Weak transcription	Monocytes-CD14+_RO01746	blood

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