Variant report

Variant	rs73500190
Chromosome Location	chr13:52724592-52724593
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs60691453	1.00[AMR][1000 genomes]
rs7319489	1.00[AMR][1000 genomes]
rs73498200	0.90[AFR][1000 genomes]
rs73500103	1.00[AFR][1000 genomes]
rs73500148	1.00[AMR][1000 genomes]
rs73500159	1.00[AMR][1000 genomes]
rs73500175	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500179	1.00[AMR][1000 genomes]
rs73500184	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73500199	1.00[AMR][1000 genomes]
rs73500200	1.00[AMR][1000 genomes]
rs73502322	1.00[AMR][1000 genomes]
rs7999934	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv1037567	chr13:52643647-52802799	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	esv3429935	chr13:52694751-52735744	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52703600-52725200	Weak transcription	Right Ventricle	heart
2	chr13:52703600-52725200	Weak transcription	Small Intestine	intestine
3	chr13:52703600-52725600	Weak transcription	Fetal Brain Male	brain
4	chr13:52703600-52730800	Weak transcription	Stomach Mucosa	stomach
5	chr13:52703600-52731000	Weak transcription	Brain Angular Gyrus	brain
6	chr13:52703600-52732600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr13:52703600-52732800	Weak transcription	Psoas Muscle	Psoas
8	chr13:52703600-52733000	Weak transcription	Esophagus	oesophagus
9	chr13:52703800-52724800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr13:52703800-52731200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr13:52703800-52731400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr13:52703800-52731400	Weak transcription	Spleen	Spleen
13	chr13:52703800-52732600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr13:52703800-52732600	Weak transcription	HMEC	breast
15	chr13:52703800-52733200	Weak transcription	Gastric	stomach
16	chr13:52704000-52733000	Weak transcription	Fetal Thymus	thymus
17	chr13:52704200-52725400	Weak transcription	Primary T cells from cord blood	blood
18	chr13:52704800-52727000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:52704800-52730000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr13:52706200-52731000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr13:52706600-52730800	Weak transcription	HUVEC	blood vessel
22	chr13:52706600-52731000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr13:52706600-52732600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr13:52706600-52732800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:52706600-52732800	Weak transcription	Pancreas	Pancrea
26	chr13:52707200-52725200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr13:52707400-52724800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr13:52707400-52725000	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr13:52707400-52725200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr13:52707400-52725600	Weak transcription	Fetal Heart	heart
31	chr13:52707400-52731200	Weak transcription	Primary B cells from cord blood	blood
32	chr13:52707400-52732800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr13:52707600-52731600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr13:52707600-52732600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr13:52707800-52724600	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr13:52707800-52732600	Weak transcription	A549	lung
37	chr13:52708000-52725400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr13:52708000-52732600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr13:52708200-52724600	Weak transcription	NH-A	brain
40	chr13:52708200-52725200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr13:52708200-52725200	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr13:52708200-52725600	Weak transcription	NHLF	lung
43	chr13:52708400-52732600	Weak transcription	HSMMtube	muscle
44	chr13:52708400-52732800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr13:52710000-52725200	Weak transcription	Left Ventricle	heart
46	chr13:52710400-52724800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr13:52710400-52724800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr13:52710400-52725000	Weak transcription	Osteobl	bone
49	chr13:52710400-52725200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr13:52710400-52725400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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