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]
rs16949912	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56021066	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56081055	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56214360	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56745423	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57783318	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58620285	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60160304	1.00[EUR][1000 genomes]
rs7326815	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7330454	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7331263	0.96[EUR][1000 genomes]
rs73543042	0.88[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	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557852	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557889	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557896	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73557899	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73559736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73559740	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74103971	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs74103990	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7985219	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs927797	0.88[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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16949906	FABP4	trans	brain	seeQTL

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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