Variant report

Variant	rs10865283
Chromosome Location	chr2:54621005-54621006
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10198148	0.92[AMR][1000 genomes]
rs10198625	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10203844	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10779939	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11125538	0.81[AMR][1000 genomes]
rs11674998	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12713257	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13392262	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34748765	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3951717	0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4233947	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4233948	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4359699	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4417755	0.87[AMR][1000 genomes]
rs4450644	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4588223	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4671213	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4671214	0.94[AMR][1000 genomes]
rs4671215	0.96[AMR][1000 genomes]
rs4671923	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4671924	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4671926	0.96[AMR][1000 genomes]
rs4671928	0.96[AMR][1000 genomes]
rs6545401	0.92[AMR][1000 genomes]
rs6545403	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6710292	0.96[AMR][1000 genomes]
rs6718253	0.82[AMR][1000 genomes]
rs6748228	0.99[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6760027	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7565489	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7576075	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7592359	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7592641	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7595929	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7597837	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7601198	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8179723	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9677336	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9677338	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9677960	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9679192	0.92[AMR][1000 genomes];0.84[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	nsv1003205	chr2:54220049-54700843	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv2762639	chr2:54220049-54700855	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1011790	chr2:54220049-54714553	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1002891	chr2:54227005-54682169	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv535722	chr2:54227005-54682169	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1011690	chr2:54255361-54700843	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv532512	chr2:54453210-54630755	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr2:54615400-54621800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr2:54615400-54623000	Weak transcription	Lung	lung
3	chr2:54615400-54643000	Weak transcription	Right Ventricle	heart
4	chr2:54615600-54621400	Weak transcription	Osteobl	bone
5	chr2:54615600-54627800	Weak transcription	Ovary	ovary
6	chr2:54615800-54621400	Weak transcription	NHDF-Ad	bronchial
7	chr2:54615800-54621800	Weak transcription	NHLF	lung
8	chr2:54618400-54621200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:54618400-54621800	Weak transcription	Brain Substantia Nigra	brain
10	chr2:54618600-54627800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:54618600-54647200	Weak transcription	Left Ventricle	heart
12	chr2:54618800-54621400	Weak transcription	Adipose Nuclei	Adipose
13	chr2:54620400-54621400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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