Variant report

Variant	rs55683917
Chromosome Location	chr8:9976479-9976480
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12678797	0.81[AMR][1000 genomes]
rs12678800	0.81[AMR][1000 genomes]
rs13254175	0.81[AMR][1000 genomes]
rs13259465	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1484641	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17689007	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17689037	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17689289	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17746227	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17746245	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34748716	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34990153	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3885723	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4841282	0.80[AMR][1000 genomes]
rs60384372	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6601414	0.80[AMR][1000 genomes]
rs6601415	0.80[AMR][1000 genomes]
rs6983332	0.81[AMR][1000 genomes]
rs6985941	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6986885	0.82[AMR][1000 genomes]
rs6986911	0.81[AMR][1000 genomes]
rs6995837	0.81[AMR][1000 genomes]
rs6995859	0.81[AMR][1000 genomes]
rs7843924	0.81[AMR][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	nsv916493	chr8:9806580-10029482	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv610263	chr8:9941021-10090149	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1034343	chr8:9948342-10014155	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv831230	chr8:9953343-10139350	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1027280	chr8:9958259-10058984	Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1021921	chr8:9958259-10212555	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv1850829	chr8:9958321-10045451	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9967200-9977400	Weak transcription	Fetal Brain Female	brain
2	chr8:9970600-9995800	Weak transcription	Pancreas	Pancrea
3	chr8:9973200-9976800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:9974400-9979600	Weak transcription	Esophagus	oesophagus
5	chr8:9975600-9987400	Weak transcription	Brain Germinal Matrix	brain

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