Variant report

Variant	rs59582715
Chromosome Location	chr10:93886447-93886448
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:93881358..93883169-chr10:93884864..93886864,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs35412677	0.89[AMR][1000 genomes]
rs57762009	0.89[AMR][1000 genomes]
rs58708663	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59509997	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6583800	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7074872	0.89[AMR][1000 genomes]
rs7075257	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7084837	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7096690	0.89[AMR][1000 genomes]
rs73314344	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316068	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316069	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316082	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73318015	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73318028	0.89[AMR][1000 genomes]
rs7907888	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051226	chr10:93711296-93915586	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv540745	chr10:93711296-93915586	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv975763	chr10:93822289-94105956	Enhancers Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1046258	chr10:93866969-94466106	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93859200-93901400	Weak transcription	Primary B cells from cord blood	blood
2	chr10:93868000-93901800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:93871000-93887200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr10:93874600-93899600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr10:93884400-93887400	Enhancers	Left Ventricle	heart
6	chr10:93884400-93890600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr10:93884800-93886600	Enhancers	HepG2	liver
8	chr10:93884800-93896400	Weak transcription	Fetal Intestine Small	intestine
9	chr10:93884800-93896800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr10:93885200-93891000	Weak transcription	Small Intestine	intestine
11	chr10:93885200-93896200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr10:93885400-93891200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr10:93885400-93902000	Weak transcription	NHLF	lung
14	chr10:93885400-93902200	Weak transcription	Brain Angular Gyrus	brain
15	chr10:93885400-93902200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr10:93885400-93902400	Weak transcription	Brain Substantia Nigra	brain
17	chr10:93885400-93906400	Weak transcription	Aorta	Aorta
18	chr10:93885400-93906600	Weak transcription	Spleen	Spleen
19	chr10:93885400-93908400	Weak transcription	Lung	lung
20	chr10:93885600-93897800	Weak transcription	Gastric	stomach
21	chr10:93885600-93902200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr10:93885800-93887200	Enhancers	Liver	Liver
23	chr10:93885800-93896600	Weak transcription	Fetal Stomach	stomach
24	chr10:93885800-93905600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr10:93886000-93902000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr10:93886200-93889600	Weak transcription	Right Atrium	heart
27	chr10:93886200-93896800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr10:93886200-93896800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr10:93886200-93902200	Weak transcription	Brain Anterior Caudate	brain
30	chr10:93886200-93906000	Weak transcription	Esophagus	oesophagus
31	chr10:93886200-93906400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr10:93886200-93906600	Weak transcription	Right Ventricle	heart
33	chr10:93886200-93907800	Weak transcription	Psoas Muscle	Psoas
34	chr10:93886200-93910800	Weak transcription	Pancreas	Pancrea
35	chr10:93886200-93911600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr10:93886400-93888600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:93886400-93890800	Weak transcription	Fetal Heart	heart
38	chr10:93886400-93891200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr10:93886400-93896600	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr10:93886400-93901800	Weak transcription	Hela-S3	cervix

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