Variant report

Variant	rs16959556
Chromosome Location	chr16:12511737-12511738
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1019576	0.90[EUR][1000 genomes]
rs10852347	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10852348	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11075070	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11075071	0.81[EUR][1000 genomes]
rs11641304	0.88[EUR][1000 genomes]
rs11862378	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11864693	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12444071	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12922243	0.86[EUR][1000 genomes]
rs12924360	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12926672	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12927878	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12932170	0.83[EUR][1000 genomes]
rs12932341	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1477119	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16959555	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1974905	0.90[EUR][1000 genomes]
rs2098761	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2865239	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3851015	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4780427	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4780428	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4780429	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4780431	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4780432	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4780433	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4781222	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4781225	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4781226	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4781227	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4781229	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4781232	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4781233	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4781235	0.82[EUR][1000 genomes]
rs6498286	0.86[EUR][1000 genomes]
rs6498288	0.89[EUR][1000 genomes]
rs6498289	0.90[EUR][1000 genomes]
rs6498292	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6498293	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6498294	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6498295	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6498296	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7187130	0.87[EUR][1000 genomes]
rs7187688	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7190294	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7192229	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7192339	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7192549	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7193128	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7198141	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7198154	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7199220	0.90[EUR][1000 genomes]
rs8043724	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8046923	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8047108	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8047934	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8049186	0.87[EUR][1000 genomes]
rs8052297	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8053319	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8061365	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8062594	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs889809	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs889810	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs889811	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9745308	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9746199	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9746397	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9746403	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][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	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	nsv457411	chr16:12363304-12520199	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv571462	chr16:12363304-12520199	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	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
5	nsv1045385	chr16:12376389-12517006	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv542748	chr16:12376389-12517006	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1736	chr16:12477807-12522707	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	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
9	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

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12476000-12531600	Weak transcription	Right Ventricle	heart
2	chr16:12497800-12519600	Weak transcription	Brain Anterior Caudate	brain
3	chr16:12497800-12539800	Weak transcription	Left Ventricle	heart
4	chr16:12498000-12515400	Weak transcription	Pancreas	Pancrea
5	chr16:12498000-12518600	Weak transcription	Fetal Intestine Small	intestine
6	chr16:12498000-12541200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr16:12498200-12513200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr16:12498200-12517200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr16:12498400-12513800	Weak transcription	Aorta	Aorta
10	chr16:12498400-12514200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr16:12498400-12514800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr16:12498400-12516200	Weak transcription	Fetal Stomach	stomach
13	chr16:12498400-12518800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr16:12498400-12523200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr16:12498400-12523600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr16:12498400-12523800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr16:12498400-12564600	Weak transcription	Esophagus	oesophagus
18	chr16:12498800-12516600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr16:12498800-12523800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr16:12499200-12511800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr16:12499200-12518200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr16:12499400-12512800	Weak transcription	Brain Substantia Nigra	brain
23	chr16:12499400-12517200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr16:12499400-12527000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr16:12499600-12512800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr16:12501800-12514000	Weak transcription	NHEK	skin
27	chr16:12501800-12514200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr16:12501800-12515600	Weak transcription	NHDF-Ad	bronchial
29	chr16:12501800-12519600	Weak transcription	Brain Hippocampus Middle	brain
30	chr16:12502000-12516000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr16:12502200-12512800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr16:12502200-12515400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr16:12506200-12529600	Weak transcription	Gastric	stomach
34	chr16:12506600-12513600	Weak transcription	Adipose Nuclei	Adipose
35	chr16:12507000-12514400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:12507400-12515400	Weak transcription	HSMMtube	muscle
37	chr16:12507600-12519200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:12507600-12527600	Weak transcription	GM12878-XiMat	blood
39	chr16:12507800-12515600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr16:12507800-12519000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr16:12508800-12523200	Weak transcription	Primary hematopoietic stem cells	blood
42	chr16:12509000-12516800	Enhancers	Placenta	Placenta
43	chr16:12509600-12513600	Weak transcription	Primary T cells from cord blood	blood
44	chr16:12509800-12511800	Weak transcription	Thymus	Thymus
45	chr16:12510000-12512600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr16:12510200-12513000	Weak transcription	Primary B cells from cord blood	blood
47	chr16:12510200-12515600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr16:12510200-12523000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr16:12510600-12511800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr16:12510600-12512000	Enhancers	HUVEC	blood vessel

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