Variant report

Variant	rs8059085
Chromosome Location	chr16:12644529-12644530
allele	A/G
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:36)

rs_ID	r²[population]
rs12444976	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1540277	0.84[AMR][1000 genomes]
rs16959823	1.00[ASN][1000 genomes]
rs169774	1.00[ASN][1000 genomes]
rs1794305	1.00[ASN][1000 genomes]
rs184127	1.00[ASN][1000 genomes]
rs1894967	1.00[ASN][1000 genomes]
rs210723	1.00[ASN][1000 genomes]
rs2157063	1.00[ASN][1000 genomes]
rs28697103	1.00[ASN][1000 genomes]
rs4781245	1.00[ASN][1000 genomes]
rs4781258	1.00[ASN][1000 genomes]
rs56275803	1.00[ASN][1000 genomes]
rs59416912	1.00[ASN][1000 genomes]
rs62028167	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62028255	1.00[ASN][1000 genomes]
rs62028256	1.00[ASN][1000 genomes]
rs62028257	1.00[ASN][1000 genomes]
rs62028660	1.00[ASN][1000 genomes]
rs6416654	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6498319	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7198031	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7200834	1.00[ASN][1000 genomes]
rs72775223	1.00[ASN][1000 genomes]
rs72775229	1.00[ASN][1000 genomes]
rs72775241	1.00[ASN][1000 genomes]
rs74009122	1.00[ASN][1000 genomes]
rs74009123	1.00[ASN][1000 genomes]
rs8055769	1.00[ASN][1000 genomes]
rs8057255	0.82[EUR][1000 genomes]
rs8060370	1.00[ASN][1000 genomes]
rs8061129	1.00[ASN][1000 genomes]
rs8061662	1.00[ASN][1000 genomes]
rs8062191	1.00[ASN][1000 genomes]
rs8062915	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9924730	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv571463	chr16:12367791-12783535	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1051242	chr16:12482972-12897243	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv542749	chr16:12482972-12897243	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1035581	chr16:12516946-12863700	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1051607	chr16:12522130-13347676	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription 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	19 gene(s)	inside rSNPs	diseases
7	nsv542750	chr16:12522130-13347676	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv1054084	chr16:12625727-12650247	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv431433	chr16:12628409-12654408	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv1842867	chr16:12632286-12678721	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1040887	chr16:12632918-12650247	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	esv2751546	chr16:12635498-12674704	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv1040358	chr16:12636982-12650247	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1050004	chr16:12641649-12654618	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv9348	chr16:12642414-12649190	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
2	chr16:12632800-12646600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr16:12632800-12663800	Weak transcription	Aorta	Aorta
4	chr16:12633000-12646600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr16:12633400-12654400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr16:12638800-12645400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr16:12639400-12645000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:12639400-12646800	Weak transcription	Brain Angular Gyrus	brain
9	chr16:12639400-12659000	Weak transcription	Lung	lung
10	chr16:12639600-12645800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr16:12640000-12647200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr16:12640600-12646000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr16:12641200-12646000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr16:12641200-12646600	Weak transcription	Brain Substantia Nigra	brain
15	chr16:12641200-12667000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr16:12641400-12644600	Weak transcription	Thymus	Thymus
17	chr16:12641600-12646400	Enhancers	Primary T cells fromperipheralblood	blood
18	chr16:12642000-12645600	Weak transcription	HSMMtube	muscle
19	chr16:12642000-12646600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr16:12642000-12662200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr16:12642200-12655000	Weak transcription	Spleen	Spleen
22	chr16:12642400-12644600	Weak transcription	Fetal Thymus	thymus
23	chr16:12642400-12653000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr16:12642800-12644800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr16:12642800-12646600	Weak transcription	Brain Hippocampus Middle	brain
26	chr16:12643000-12645200	Weak transcription	Esophagus	oesophagus
27	chr16:12643000-12659200	Weak transcription	Placenta	Placenta
28	chr16:12643200-12653000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:12643600-12646000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr16:12643600-12646200	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr16:12643800-12645600	Weak transcription	Gastric	stomach
32	chr16:12644000-12645000	Weak transcription	GM12878-XiMat	blood
33	chr16:12644000-12645800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr16:12644000-12646200	Enhancers	Primary T cells from cord blood	blood
35	chr16:12644200-12645400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr16:12644200-12646000	Enhancers	Primary B cells from peripheral blood	blood
37	chr16:12644200-12646000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr16:12644200-12646000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr16:12644200-12646200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr16:12644400-12645000	Weak transcription	Primary B cells from cord blood	blood

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