Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50448759..50451494-chr10:50463430..50466103,2	K562	blood:
2	chr10:50443853..50446189-chr10:50448741..50451708,2	K562	blood:

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10857444	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10857451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101012	1.00[AMR][1000 genomes]
rs11101013	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11101020	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11101030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101034	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11101051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11593489	0.87[EUR][1000 genomes]
rs12354761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12355572	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41280543	1.00[AMR][1000 genomes]
rs41281945	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50447600-50452400	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr10:50447600-50453000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr10:50448800-50450400	Enhancers	Fetal Stomach	stomach
4	chr10:50449000-50451000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr10:50449000-50451000	Enhancers	Fetal Muscle Trunk	muscle
6	chr10:50449000-50451200	Enhancers	Fetal Muscle Leg	muscle
7	chr10:50449000-50451400	Enhancers	Left Ventricle	heart
8	chr10:50449000-50451400	Enhancers	Right Atrium	heart
9	chr10:50449000-50451600	Enhancers	Fetal Heart	heart
10	chr10:50449000-50451600	Enhancers	Right Ventricle	heart
11	chr10:50449400-50450600	Weak transcription	Liver	Liver
12	chr10:50449400-50451200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr10:50449600-50450800	Weak transcription	Primary B cells from cord blood	blood
14	chr10:50449600-50451000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr10:50449600-50451200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:50449800-50451600	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr10:50449800-50451600	Enhancers	K562	blood
18	chr10:50449800-50452200	Enhancers	Spleen	Spleen
19	chr10:50450000-50450800	Weak transcription	Placenta	Placenta
20	chr10:50450000-50451800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:50450200-50451400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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