Variant report

Variant	rs2368996
Chromosome Location	chr14:104502194-104502195
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10130042	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10131031	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10131231	0.89[ASN][1000 genomes]
rs10133836	0.82[YRI][hapmap]
rs10137517	0.83[AMR][1000 genomes]
rs10137676	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10137889	0.89[ASN][1000 genomes]
rs10139210	0.89[ASN][1000 genomes]
rs10140292	1.00[JPT][hapmap]
rs10140436	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10141374	0.89[ASN][1000 genomes]
rs10142956	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10145882	1.00[JPT][hapmap]
rs10149898	0.89[ASN][1000 genomes]
rs10151165	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11160776	0.81[YRI][hapmap]
rs11160781	0.86[YRI][hapmap]
rs1187452	0.82[YRI][hapmap]
rs1187453	0.82[YRI][hapmap]
rs12436665	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12437404	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs17101922	1.00[JPT][hapmap]
rs1885596	0.82[YRI][hapmap]
rs1951583	0.90[YRI][hapmap]
rs2295662	0.89[ASN][1000 genomes]
rs2368997	0.86[YRI][hapmap]
rs28416628	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28439019	0.89[ASN][1000 genomes]
rs28514602	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28555097	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28593161	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28715405	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28841005	0.85[AMR][1000 genomes]
rs4900603	1.00[JPT][hapmap]
rs4900606	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906386	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs4906388	0.89[ASN][1000 genomes]
rs4906393	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906394	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906400	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906403	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906404	0.82[YRI][hapmap]
rs4906407	1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4906412	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4906414	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs55746000	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs55866217	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56050561	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56279366	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56872578	0.89[ASN][1000 genomes]
rs58128911	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58220415	0.89[ASN][1000 genomes]
rs59838226	0.89[ASN][1000 genomes]
rs7149117	0.82[YRI][hapmap]
rs7150795	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7155057	0.82[YRI][hapmap]
rs7161153	0.82[YRI][hapmap]
rs74086783	0.89[ASN][1000 genomes]
rs74086977	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs8004485	0.89[ASN][1000 genomes]
rs8007491	0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs8020110	1.00[JPT][hapmap]
rs9324070	1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9671924	1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.89[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	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
4	nsv1049690	chr14:104411621-104575838	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv542208	chr14:104411621-104575838	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv526680	chr14:104427043-104568472	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1047990	chr14:104460605-104556463	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv542209	chr14:104497447-104540729	Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1050479	chr14:104500427-104805738	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104492200-104516000	Weak transcription	Spleen	Spleen
2	chr14:104493000-104504000	Weak transcription	Gastric	stomach
3	chr14:104496400-104520800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:104499000-104511800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr14:104499800-104506600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:104501000-104504200	Enhancers	Fetal Brain Male	brain
7	chr14:104501200-104503800	Enhancers	Fetal Brain Female	brain
8	chr14:104501800-104502200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
9	chr14:104501800-104502200	Flanking Active TSS	Brain Germinal Matrix	brain
10	chr14:104501800-104502200	Bivalent Enhancer	Brain Hippocampus Middle	brain
11	chr14:104501800-104502200	Bivalent Enhancer	HSMMtube	muscle
12	chr14:104502000-104502200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:104502000-104502200	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links