Variant report

Variant	rs73080295
Chromosome Location	chr3:53349508-53349509
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10433617	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10433618	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1108506	0.95[EUR][1000 genomes]
rs11551405	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17030933	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17030934	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17234771	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17235667	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56654807	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58558806	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59145995	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62255989	0.83[AMR][1000 genomes]
rs62255993	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62255994	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62255999	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62256000	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62256003	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62256009	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62256043	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62256049	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62256050	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62256053	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62256962	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62256964	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62256965	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62256966	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62256968	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62256969	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62257004	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62257007	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62257009	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62257011	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62257013	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62257024	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6780100	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73080266	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73080271	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73080273	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73082274	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7622159	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9830594	0.89[EUR][1000 genomes]
rs9830895	0.91[EUR][1000 genomes]
rs9846315	0.93[EUR][1000 genomes]
rs9850440	0.92[EUR][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	nsv876801	chr3:53325905-53467506	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
2	nsv876802	chr3:53325905-53470863	Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53309400-53351200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:53322400-53353600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:53326600-53364400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr3:53327200-53358200	Weak transcription	K562	blood
5	chr3:53332600-53355600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:53334600-53355200	Strong transcription	Fetal Stomach	stomach
7	chr3:53334600-53358400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:53335400-53354200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr3:53338000-53351400	Weak transcription	Right Atrium	heart
10	chr3:53338000-53374000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr3:53338200-53352000	Weak transcription	Colonic Mucosa	Colon
12	chr3:53338200-53352600	Weak transcription	A549	lung
13	chr3:53338200-53355200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:53338200-53380200	Weak transcription	Fetal Brain Male	brain
15	chr3:53338400-53367400	Weak transcription	Small Intestine	intestine
16	chr3:53341000-53353200	Strong transcription	Primary T cells from cord blood	blood
17	chr3:53341200-53353200	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr3:53341200-53354800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr3:53342600-53354000	Strong transcription	Duodenum Mucosa	Duodenum
20	chr3:53344000-53354400	Weak transcription	Psoas Muscle	Psoas
21	chr3:53344000-53364200	Weak transcription	Right Ventricle	heart
22	chr3:53344600-53355600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:53344600-53358200	Weak transcription	Pancreas	Pancrea
24	chr3:53345600-53351400	Weak transcription	NHDF-Ad	bronchial
25	chr3:53345600-53352000	Weak transcription	Colon Smooth Muscle	Colon
26	chr3:53345800-53357800	Strong transcription	Fetal Intestine Small	intestine
27	chr3:53345800-53362600	Weak transcription	NHLF	lung
28	chr3:53346000-53352600	Weak transcription	HSMM	muscle
29	chr3:53346000-53373600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr3:53346200-53351400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr3:53346200-53352800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:53346200-53365200	Weak transcription	Fetal Kidney	kidney
33	chr3:53346200-53378600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr3:53346400-53350200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr3:53346400-53350200	Weak transcription	Fetal Lung	lung
36	chr3:53346400-53350200	Weak transcription	Osteobl	bone
37	chr3:53346400-53350600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr3:53346400-53351200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:53346400-53351200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:53346400-53351200	Weak transcription	Adipose Nuclei	Adipose
41	chr3:53346400-53351200	Weak transcription	Left Ventricle	heart
42	chr3:53346400-53351200	Weak transcription	Ovary	ovary
43	chr3:53346400-53351200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr3:53346400-53351200	Weak transcription	HUVEC	blood vessel
45	chr3:53346400-53351400	Weak transcription	Gastric	stomach
46	chr3:53346400-53351400	Weak transcription	Lung	lung
47	chr3:53346400-53351800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:53346400-53351800	Weak transcription	Brain Germinal Matrix	brain
49	chr3:53346400-53352000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr3:53346400-53352000	Weak transcription	Esophagus	oesophagus

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