Variant report

Variant	rs11851834
Chromosome Location	chr14:83694961-83694962
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1039548	0.92[EUR][1000 genomes]
rs10484150	0.87[EUR][1000 genomes]
rs10873345	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11159572	0.85[EUR][1000 genomes]
rs11159578	0.84[ASN][1000 genomes]
rs1154828	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11628262	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11847743	0.86[EUR][1000 genomes]
rs11849865	0.87[EUR][1000 genomes]
rs11849894	0.87[EUR][1000 genomes]
rs11851374	0.84[ASN][1000 genomes]
rs12586213	0.87[EUR][1000 genomes]
rs12587595	0.85[EUR][1000 genomes]
rs12587751	0.80[CEU][hapmap]
rs1263441	0.85[EUR][1000 genomes]
rs1263442	0.85[EUR][1000 genomes]
rs1263443	0.85[EUR][1000 genomes]
rs1263445	0.85[EUR][1000 genomes]
rs12878955	0.87[EUR][1000 genomes]
rs12882063	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1379244	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1457017	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1457018	0.87[EUR][1000 genomes]
rs1888559	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2124850	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2124852	0.96[EUR][1000 genomes]
rs2372314	0.86[EUR][1000 genomes]
rs2372316	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36014939	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4904107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6574740	0.87[EUR][1000 genomes]
rs6574741	0.87[EUR][1000 genomes]
rs7143426	0.85[EUR][1000 genomes]
rs7146298	0.87[EUR][1000 genomes]
rs7146647	0.87[EUR][1000 genomes]
rs7152994	0.85[EUR][1000 genomes]
rs7157948	0.86[EUR][1000 genomes]
rs7158248	0.86[EUR][1000 genomes]
rs8005336	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8009267	0.87[EUR][1000 genomes]
rs8009891	0.87[EUR][1000 genomes]
rs8010665	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs977975	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902127	chr14:83524701-83746190	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1041909	chr14:83532477-83904217	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv542148	chr14:83532477-83904217	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv902134	chr14:83562841-83725177	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv902135	chr14:83583841-83725177	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv902140	chr14:83591673-83725177	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv902145	chr14:83618392-83746190	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv902146	chr14:83618392-83756424	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1052933	chr14:83626090-83785690	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv542149	chr14:83626090-83785690	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv456351	chr14:83632616-83719652	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv565366	chr14:83632616-83719652	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv565367	chr14:83632616-83780605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv1037255	chr14:83638819-83814438	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	nsv542150	chr14:83638819-83814438	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	nsv1042759	chr14:83640727-83706596	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1052145	chr14:83650210-83700488	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv902147	chr14:83650541-83746190	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv902148	chr14:83650541-83756424	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv565368	chr14:83658723-83719652	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv902149	chr14:83658723-83746190	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv902150	chr14:83665111-83746190	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv1054422	chr14:83667129-83729518	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv542151	chr14:83667129-83729518	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv902151	chr14:83673387-83746190	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:83694400-83696200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:83694400-83697400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr14:83694400-83698600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr14:83694600-83695800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr14:83694600-83696200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr14:83694800-83696000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr14:83694800-83696400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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