Variant report

Variant	rs73214666
Chromosome Location	chr8:19496895-19496896
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10086135	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13275011	0.85[EUR][1000 genomes]
rs55651857	0.89[EUR][1000 genomes]
rs55659028	0.89[EUR][1000 genomes]
rs55726693	0.96[EUR][1000 genomes]
rs55898253	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56167026	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214663	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214667	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73214668	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214672	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214675	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214677	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214684	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73214687	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
2	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv890627	chr8:19389865-19561997	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv610754	chr8:19419494-19525294	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1021575	chr8:19430653-19623452	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1025271	chr8:19435147-19574969	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1015448	chr8:19474715-19520367	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19482000-19520000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr8:19485400-19499200	Weak transcription	Placenta	Placenta
3	chr8:19485400-19500000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:19488800-19501200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr8:19489000-19497800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr8:19489800-19500000	Weak transcription	Lung	lung
7	chr8:19490800-19497200	Weak transcription	Hela-S3	cervix
8	chr8:19491400-19499200	Weak transcription	Fetal Lung	lung
9	chr8:19493400-19497000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:19494200-19497600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:19495000-19497600	Genic enhancers	A549	lung
12	chr8:19495000-19498600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr8:19495200-19497400	Enhancers	Brain Cingulate Gyrus	brain
14	chr8:19495200-19497600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:19495200-19497800	Enhancers	Brain Substantia Nigra	brain
16	chr8:19495200-19498000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chr8:19495200-19498400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr8:19495400-19497600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:19495600-19497200	Enhancers	Brain Anterior Caudate	brain
20	chr8:19495600-19497800	Enhancers	Primary B cells from peripheral blood	blood
21	chr8:19495600-19497800	Enhancers	Brain Hippocampus Middle	brain
22	chr8:19495600-19497800	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr8:19495600-19498000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chr8:19495600-19500400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:19495800-19497600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr8:19495800-19497800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
27	chr8:19495800-19500200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr8:19495800-19508600	Weak transcription	Primary T cells from cord blood	blood
29	chr8:19496000-19498200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:19496000-19498600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr8:19496000-19498600	Weak transcription	Left Ventricle	heart
32	chr8:19496000-19499200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:19496000-19501200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr8:19496000-19502400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr8:19496000-19503000	Weak transcription	Pancreas	Pancrea
36	chr8:19496000-19503000	Weak transcription	Right Atrium	heart
37	chr8:19496000-19503000	Weak transcription	Spleen	Spleen
38	chr8:19496000-19504200	Weak transcription	Right Ventricle	heart
39	chr8:19496200-19497000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr8:19496200-19500200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr8:19496200-19502600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr8:19496400-19498400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr8:19496600-19497000	Enhancers	HepG2	liver
44	chr8:19496600-19497200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr8:19496600-19497400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
46	chr8:19496600-19497400	Enhancers	Brain Angular Gyrus	brain
47	chr8:19496600-19499200	Weak transcription	HUVEC	blood vessel
48	chr8:19496800-19497800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr8:19496800-19499000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:19496800-19501600	Weak transcription	Primary B cells from cord blood	blood

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