Variant report

Variant	rs9573659
Chromosome Location	chr13:76354291-76354292
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1036869	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1570556	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2031241	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2031242	0.84[ASN][1000 genomes]
rs2120067	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2120068	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2274062	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4885348	0.84[EUR][1000 genomes]
rs4885349	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7139507	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7320900	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7321748	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7322414	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7326714	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7331429	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7992526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9530467	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9544043	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9573658	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][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	nsv949152	chr13:76211453-76366622	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	esv2758333	chr13:76321610-76542003	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	esv2759950	chr13:76321610-76542003	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76323800-76356600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:76338000-76356800	Weak transcription	Brain Anterior Caudate	brain
3	chr13:76338000-76362800	Weak transcription	Fetal Stomach	stomach
4	chr13:76338600-76356600	Weak transcription	Left Ventricle	heart
5	chr13:76338800-76371000	Weak transcription	Fetal Thymus	thymus
6	chr13:76340000-76363600	Weak transcription	Thymus	Thymus
7	chr13:76342400-76357800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr13:76343400-76370800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr13:76344800-76356800	Weak transcription	Fetal Lung	lung
10	chr13:76346800-76361600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr13:76347400-76358000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr13:76347400-76361400	Weak transcription	HMEC	breast
13	chr13:76347800-76356400	Weak transcription	NH-A	brain
14	chr13:76347800-76356600	Weak transcription	HSMMtube	muscle
15	chr13:76347800-76356800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr13:76347800-76361400	Weak transcription	Gastric	stomach
17	chr13:76348200-76354400	Weak transcription	Fetal Intestine Large	intestine
18	chr13:76348400-76356600	Weak transcription	Liver	Liver
19	chr13:76348600-76355200	Strong transcription	Osteobl	bone
20	chr13:76349000-76356800	Weak transcription	NHLF	lung
21	chr13:76350000-76371000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr13:76350200-76358000	Weak transcription	Small Intestine	intestine
23	chr13:76350600-76361200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr13:76351200-76356600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr13:76351400-76354600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr13:76351400-76356600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr13:76351400-76360200	Weak transcription	Right Ventricle	heart
28	chr13:76351600-76356600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr13:76351800-76356800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:76352600-76355000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr13:76352600-76355000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr13:76352600-76355200	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr13:76352800-76357200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr13:76353000-76355200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr13:76353400-76356400	Weak transcription	Hela-S3	cervix
36	chr13:76353400-76356600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr13:76353400-76362800	Weak transcription	Lung	lung
38	chr13:76353400-76370600	Weak transcription	Primary T cells from cord blood	blood
39	chr13:76353600-76355000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr13:76353800-76356200	Weak transcription	HSMM	muscle
41	chr13:76353800-76356600	Weak transcription	NHDF-Ad	bronchial
42	chr13:76353800-76357200	Weak transcription	HepG2	liver
43	chr13:76353800-76357600	Weak transcription	A549	lung
44	chr13:76354000-76356600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr13:76354200-76355000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung

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