Variant report

Variant	rs13360956
Chromosome Location	chr5:115753240-115753241
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs17139822	1.00[EUR][1000 genomes]
rs1863988	1.00[EUR][1000 genomes]
rs1963859	1.00[EUR][1000 genomes]
rs57331771	1.00[EUR][1000 genomes]
rs57894479	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58112531	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59453842	1.00[EUR][1000 genomes]
rs59710297	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59909017	1.00[EUR][1000 genomes]
rs60032314	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60114388	1.00[AMR][1000 genomes]
rs60372854	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60456887	1.00[EUR][1000 genomes]
rs73261038	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73261052	1.00[AMR][1000 genomes]
rs73261087	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263025	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263035	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263038	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263052	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263071	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73263076	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73264977	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73264993	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266806	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266818	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266825	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266826	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266833	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266838	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73266864	1.00[AMR][1000 genomes]
rs73268917	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268920	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268927	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268929	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268948	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268952	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268959	1.00[EUR][1000 genomes]
rs73268964	1.00[EUR][1000 genomes]
rs73268967	1.00[EUR][1000 genomes]
rs73268975	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268979	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268984	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73268993	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73270707	1.00[EUR][1000 genomes]
rs73270746	1.00[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	esv1845769	chr5:115730278-115763979	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115708600-115754000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:115723000-115776000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr5:115723600-115784800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr5:115730400-115769600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:115731000-115757000	Weak transcription	Gastric	stomach
6	chr5:115732600-115760200	Weak transcription	Liver	Liver
7	chr5:115733800-115754400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr5:115734200-115755200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr5:115736200-115753600	Weak transcription	Primary B cells from peripheral blood	blood
10	chr5:115746800-115756600	Strong transcription	Primary T cells from cord blood	blood
11	chr5:115747200-115760000	Weak transcription	Right Ventricle	heart
12	chr5:115747400-115753600	Weak transcription	Psoas Muscle	Psoas
13	chr5:115747400-115755000	Weak transcription	Right Atrium	heart
14	chr5:115747400-115760800	Weak transcription	Left Ventricle	heart
15	chr5:115747400-115760800	Weak transcription	Pancreas	Pancrea
16	chr5:115747600-115756000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:115747800-115757600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr5:115747800-115764200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr5:115747800-115765600	Weak transcription	Lung	lung
20	chr5:115748000-115754800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr5:115748400-115756000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr5:115748600-115783000	Weak transcription	Thymus	Thymus
23	chr5:115749400-115753400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:115749400-115782000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr5:115750200-115779400	Weak transcription	Fetal Intestine Small	intestine
26	chr5:115751200-115758800	Strong transcription	Primary B cells from cord blood	blood
27	chr5:115751600-115756400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr5:115751600-115757800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr5:115751600-115774800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr5:115752000-115757000	Weak transcription	Spleen	Spleen
31	chr5:115752400-115754600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr5:115752400-115756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr5:115752800-115779400	Weak transcription	Fetal Intestine Large	intestine

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