Variant report

Variant	rs58031076
Chromosome Location	chr16:12460944-12460945
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-276H1.3.1-2	chr16:12460839-12461326	ENSG00000261394.1
2	lnc-RP11-276H1.3.1-2	chr16:12460012-12461326	NONHSAT140620

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12103021	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13331380	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13332083	0.86[EUR][1000 genomes]
rs13332306	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16959350	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28368750	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28372578	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28405384	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28462125	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28472378	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28496413	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28605678	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55916220	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56666563	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56836971	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57011047	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58393449	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60011426	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60663572	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61159108	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73508005	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74008988	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74008989	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74009002	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs746311	0.86[EUR][1000 genomes]
rs746312	0.86[EUR][1000 genomes]
rs9922894	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9926796	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9929445	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9932158	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9933058	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv833141	chr16:12314613-12487992	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12410200-12464800	Weak transcription	Gastric	stomach
2	chr16:12428400-12461200	Weak transcription	Thymus	Thymus
3	chr16:12435800-12484000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:12443600-12470800	Weak transcription	HepG2	liver
5	chr16:12444800-12491400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr16:12447600-12470000	Weak transcription	Esophagus	oesophagus
7	chr16:12448600-12471200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr16:12449800-12463000	Strong transcription	Primary B cells from peripheral blood	blood
9	chr16:12450800-12470000	Weak transcription	Fetal Thymus	thymus
10	chr16:12452800-12464200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr16:12453000-12461000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr16:12453000-12470600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr16:12453200-12479000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr16:12453400-12467400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr16:12453400-12469400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr16:12454400-12469200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:12454600-12470800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr16:12455600-12479400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:12456200-12470600	Weak transcription	NHEK	skin
20	chr16:12456800-12478600	Weak transcription	Ovary	ovary
21	chr16:12457000-12492400	Weak transcription	Lung	lung
22	chr16:12457200-12465000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr16:12457400-12462000	Weak transcription	Fetal Heart	heart
24	chr16:12457400-12462200	Weak transcription	Left Ventricle	heart
25	chr16:12457400-12469000	Weak transcription	Brain Angular Gyrus	brain
26	chr16:12457400-12469000	Weak transcription	Brain Anterior Caudate	brain
27	chr16:12457400-12469200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr16:12457400-12497400	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr16:12457600-12464400	Weak transcription	Right Atrium	heart
30	chr16:12457600-12464600	Weak transcription	Adipose Nuclei	Adipose
31	chr16:12457600-12491600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr16:12457600-12497400	Weak transcription	Spleen	Spleen
33	chr16:12458000-12462000	Strong transcription	Primary T cells from cord blood	blood
34	chr16:12458800-12461000	Weak transcription	Primary B cells from cord blood	blood
35	chr16:12460000-12461000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:12460000-12461000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr16:12460000-12461000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr16:12460000-12461000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr16:12460000-12461200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr16:12460200-12461000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr16:12460200-12461000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr16:12460200-12461000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr16:12460200-12461000	Enhancers	Brain Cingulate Gyrus	brain
44	chr16:12460200-12461000	Enhancers	Brain Hippocampus Middle	brain
45	chr16:12460200-12461000	Enhancers	Brain Substantia Nigra	brain
46	chr16:12460400-12461000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr16:12460400-12461200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr16:12460800-12461200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr16:12460800-12461200	Strong transcription	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links