Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:95165821..95169962-chr13:95170967..95173736,3	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs16949906	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16949912	1.00[EUR][1000 genomes]
rs56021066	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56081055	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56214360	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56745423	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57783318	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58620285	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60160304	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7326815	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7330454	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7331263	0.96[EUR][1000 genomes]
rs73543042	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73544881	0.93[EUR][1000 genomes]
rs73544886	0.93[EUR][1000 genomes]
rs73546604	0.96[EUR][1000 genomes]
rs73557842	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557852	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557889	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557896	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557899	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73559736	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73559740	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74103971	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7985219	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs927797	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS 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 miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95168600-95173400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr13:95171800-95172800	Enhancers	Brain Angular Gyrus	brain
3	chr13:95171800-95172800	Enhancers	Brain Anterior Caudate	brain
4	chr13:95171800-95172800	Enhancers	Brain Cingulate Gyrus	brain
5	chr13:95171800-95172800	Enhancers	Brain Hippocampus Middle	brain
6	chr13:95171800-95172800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr13:95171800-95173000	Enhancers	Brain Substantia Nigra	brain
8	chr13:95171800-95173400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr13:95172000-95172800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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