Variant report

Variant	rs2059627
Chromosome Location	chr15:44414958-44414959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10152607	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10851415	0.89[AMR][1000 genomes]
rs10851416	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11070419	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1115870	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1160066	0.92[EUR][1000 genomes]
rs11632901	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12324261	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12900880	0.81[EUR][1000 genomes]
rs12913809	0.89[AMR][1000 genomes]
rs1365456	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1426658	0.81[EUR][1000 genomes]
rs1808509	0.92[EUR][1000 genomes]
rs1813196	0.95[AFR][1000 genomes]
rs1820482	0.81[EUR][1000 genomes]
rs1820484	0.91[AFR][1000 genomes]
rs1834641	0.91[AFR][1000 genomes]
rs2015277	0.86[EUR][1000 genomes]
rs2019074	0.92[EUR][1000 genomes]
rs2042741	0.84[EUR][1000 genomes]
rs2059626	0.86[EUR][1000 genomes]
rs2059628	0.92[EUR][1000 genomes]
rs2114416	0.91[AFR][1000 genomes]
rs2162365	0.91[AFR][1000 genomes]
rs2162366	0.91[AFR][1000 genomes]
rs2217108	0.91[AFR][1000 genomes]
rs2412845	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2412846	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2412847	0.81[EUR][1000 genomes]
rs2412848	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2412851	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2412853	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2412854	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2555375	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2555380	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2555385	0.92[EUR][1000 genomes]
rs2555389	0.91[AFR][1000 genomes]
rs2615268	0.88[AFR][1000 genomes]
rs2615272	0.89[AFR][1000 genomes]
rs2615285	0.92[EUR][1000 genomes]
rs2615287	0.92[EUR][1000 genomes]
rs2615288	0.92[EUR][1000 genomes]
rs2615290	0.92[EUR][1000 genomes]
rs2615291	0.89[EUR][1000 genomes]
rs2615292	0.92[EUR][1000 genomes]
rs2615294	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2615295	0.92[EUR][1000 genomes]
rs2615297	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2623017	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2623019	0.89[EUR][1000 genomes]
rs2706471	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2706473	0.92[EUR][1000 genomes]
rs2706474	0.92[EUR][1000 genomes]
rs2706481	0.89[EUR][1000 genomes]
rs2706487	0.91[AFR][1000 genomes]
rs2706488	0.84[EUR][1000 genomes]
rs2733201	0.84[AFR][1000 genomes]
rs2733203	0.92[EUR][1000 genomes]
rs2733204	0.92[EUR][1000 genomes]
rs2733221	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2733226	0.89[EUR][1000 genomes]
rs28667396	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2899103	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2930528	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2957581	0.92[EUR][1000 genomes]
rs3919618	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4923969	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4923972	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4924728	0.81[EUR][1000 genomes]
rs4924729	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4924731	0.89[AMR][1000 genomes]
rs4924734	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4924735	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4924737	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6493092	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6493093	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6493094	0.81[EUR][1000 genomes]
rs7166715	0.92[EUR][1000 genomes]
rs7176955	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8033233	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8036541	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8037441	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8037596	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8041487	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9920249	0.89[AMR][1000 genomes];0.81[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	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
2	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
3	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv1052511	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv542371	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv832989	chr15:44306469-44461710	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv3351630	chr15:44334624-44547841	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv904173	chr15:44391572-44522214	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv904174	chr15:44391572-44538660	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv569298	chr15:44401266-44513090	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv904175	chr15:44403988-44538660	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv904176	chr15:44403988-44579854	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44410200-44421800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:44412600-44417600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr15:44412600-44421000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:44412800-44418200	Weak transcription	Fetal Heart	heart
5	chr15:44412800-44419000	Weak transcription	Brain Angular Gyrus	brain
6	chr15:44413200-44417600	Weak transcription	Brain Anterior Caudate	brain
7	chr15:44413400-44417600	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:44413400-44417600	Weak transcription	Brain Substantia Nigra	brain
9	chr15:44413400-44423000	Weak transcription	HMEC	breast
10	chr15:44414800-44429400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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