Variant report

Variant	rs2224259
Chromosome Location	chr20:41663461-41663462
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1157154	0.80[EUR][1000 genomes]
rs206148	0.85[EUR][1000 genomes]
rs206151	0.91[EUR][1000 genomes]
rs206152	0.87[EUR][1000 genomes]
rs206153	0.91[EUR][1000 genomes]
rs206154	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs206155	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs206156	0.88[EUR][1000 genomes]
rs206157	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs206158	0.91[EUR][1000 genomes]
rs206159	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs206161	0.89[EUR][1000 genomes]
rs206162	0.92[EUR][1000 genomes]
rs2208048	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2208049	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2425545	0.95[EUR][1000 genomes]
rs2425546	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2425547	0.95[EUR][1000 genomes]
rs2425549	0.95[EUR][1000 genomes]
rs2425550	0.95[EUR][1000 genomes]
rs2425551	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2425552	0.94[EUR][1000 genomes]
rs2425553	0.95[EUR][1000 genomes]
rs2425554	0.95[EUR][1000 genomes]
rs2425555	0.95[EUR][1000 genomes]
rs2425556	0.95[EUR][1000 genomes]
rs2425557	0.95[EUR][1000 genomes]
rs2425558	0.93[EUR][1000 genomes]
rs2425559	0.93[EUR][1000 genomes]
rs2425560	0.93[EUR][1000 genomes]
rs2425561	0.93[EUR][1000 genomes]
rs2425563	0.93[EUR][1000 genomes]
rs2425564	0.93[EUR][1000 genomes]
rs2425565	0.93[EUR][1000 genomes]
rs2425566	0.91[EUR][1000 genomes]
rs2425567	0.81[EUR][1000 genomes]
rs2425568	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2425570	0.80[EUR][1000 genomes]
rs2425572	0.80[EUR][1000 genomes]
rs2425573	0.80[EUR][1000 genomes]
rs2425574	0.80[EUR][1000 genomes]
rs2425579	0.82[AMR][1000 genomes]
rs3091443	0.93[EUR][1000 genomes]
rs3091548	0.95[EUR][1000 genomes]
rs3091580	0.93[EUR][1000 genomes]
rs3091581	0.95[EUR][1000 genomes]
rs3091752	0.93[EUR][1000 genomes]
rs3091800	0.93[EUR][1000 genomes]
rs3091990	0.93[EUR][1000 genomes]
rs3091991	0.92[EUR][1000 genomes]
rs3092095	0.93[EUR][1000 genomes]
rs3092117	0.93[EUR][1000 genomes]
rs3092177	0.93[EUR][1000 genomes]
rs3092292	0.92[EUR][1000 genomes]
rs3092328	0.95[EUR][1000 genomes]
rs3092568	0.80[EUR][1000 genomes]
rs3092739	0.93[EUR][1000 genomes]
rs4410343	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4444608	0.95[EUR][1000 genomes]
rs4812667	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6030612	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6030614	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6030615	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67112782	0.97[EUR][1000 genomes]
rs713108	0.80[EUR][1000 genomes]
rs714972	0.83[AMR][1000 genomes]
rs755148	0.83[AMR][1000 genomes]
rs755149	0.82[AMR][1000 genomes]
rs8120802	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs910829	0.93[EUR][1000 genomes]
rs910830	0.93[EUR][1000 genomes]
rs927054	0.95[EUR][1000 genomes]
rs927056	0.95[EUR][1000 genomes]
rs984962	0.80[EUR][1000 genomes]
rs998739	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063450	chr20:41409901-41880620	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1060690	chr20:41413369-41851935	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1066088	chr20:41417205-42060036	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1060468	chr20:41518010-41700012	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1061053	chr20:41521471-41704874	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv949221	chr20:41594025-41742176	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv869774	chr20:41595567-41746533	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv2762078	chr20:41598181-41745491	Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv948829	chr20:41598995-41742176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv912889	chr20:41609188-41666379	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1061219	chr20:41613071-41673335	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1065908	chr20:41620966-41735969	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41654600-41672800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr20:41658200-41664000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr20:41663400-41663600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr20:41663400-41663600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr20:41663400-41664200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr20:41663400-41664800	Enhancers	HepG2	liver

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