Variant report

Variant	rs73551414
Chromosome Location	chr6:133921583-133921584
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs55645130	1.00[AMR][1000 genomes]
rs55863046	1.00[AMR][1000 genomes]
rs55963381	1.00[AMR][1000 genomes]
rs56128814	1.00[AMR][1000 genomes]
rs56332553	1.00[AMR][1000 genomes]
rs56353427	1.00[AMR][1000 genomes]
rs56788898	1.00[AMR][1000 genomes]
rs57022180	1.00[AMR][1000 genomes]
rs58069152	1.00[AMR][1000 genomes]
rs60210492	1.00[AMR][1000 genomes]
rs6926676	1.00[AMR][1000 genomes]
rs6936392	1.00[AMR][1000 genomes]
rs73546811	1.00[AMR][1000 genomes]
rs73546832	1.00[AMR][1000 genomes]
rs73546898	1.00[AMR][1000 genomes]
rs73548873	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73548875	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73553005	1.00[AMR][1000 genomes]
rs73553023	1.00[AMR][1000 genomes]
rs73553034	1.00[AMR][1000 genomes]
rs73553036	1.00[AMR][1000 genomes]
rs73553043	1.00[AMR][1000 genomes]
rs73553058	1.00[AMR][1000 genomes]
rs73553059	1.00[AMR][1000 genomes]
rs73553068	1.00[AMR][1000 genomes]
rs73553070	1.00[AMR][1000 genomes]
rs73553072	1.00[AMR][1000 genomes]
rs73553074	1.00[AMR][1000 genomes]
rs73553075	1.00[AMR][1000 genomes]
rs73553076	1.00[AMR][1000 genomes]
rs73553084	1.00[AMR][1000 genomes]
rs73553088	1.00[AMR][1000 genomes]
rs73555309	1.00[AMR][1000 genomes]
rs73555351	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73557143	1.00[AMR][1000 genomes]
rs73557178	1.00[AMR][1000 genomes]
rs73557189	1.00[AMR][1000 genomes]
rs73559222	1.00[AMR][1000 genomes]
rs73559294	1.00[AMR][1000 genomes]
rs73776065	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73776709	1.00[AMR][1000 genomes]
rs73776715	1.00[AMR][1000 genomes]
rs7746146	1.00[AMR][1000 genomes]
rs7761492	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886682	chr6:133892208-133943732	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1019267	chr6:133912335-133975187	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv437014	chr6:133919776-133924082	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133912400-133925200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:133916000-133925200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:133917200-133925200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:133917400-133921600	Weak transcription	Fetal Lung	lung

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