Variant report

Variant	rs13072826
Chromosome Location	chr3:195064755-195064756
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10804414	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1094677	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1105165	0.82[ASN][1000 genomes]
rs11706264	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13059843	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13062518	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13072883	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13091924	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13099106	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13324903	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1538767	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2791603	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4677834	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4677835	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55672262	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55927338	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6778719	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7611238	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7633265	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7634345	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7651757	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs823300	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs823301	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs823302	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs823306	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs823310	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs823311	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs823314	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9810077	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9823964	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9840346	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
3	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
4	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
5	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	esv1832781	chr3:194902818-195528226	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
10	nsv432508	chr3:194916131-195478861	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
11	nsv432510	chr3:194935314-195478861	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
12	nsv1005519	chr3:194964301-195340515	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
13	nsv432511	chr3:194986167-195479748	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers 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 miRNA	57 gene(s)	inside rSNPs	diseases
14	nsv432512	chr3:195007260-195475989	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
15	nsv526569	chr3:195038287-195123495	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
16	nsv878138	chr3:195057001-195477791	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
17	nsv878139	chr3:195058837-195158031	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	esv1799680	chr3:195060129-195154361	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
19	nsv878140	chr3:195062395-195096625	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194992600-195090000	Weak transcription	Aorta	Aorta
2	chr3:194993000-195076000	Weak transcription	Fetal Heart	heart
3	chr3:195004000-195066600	Weak transcription	Small Intestine	intestine
4	chr3:195010000-195076400	Weak transcription	Brain Angular Gyrus	brain
5	chr3:195022600-195073400	Weak transcription	HMEC	breast
6	chr3:195022800-195073400	Weak transcription	NHEK	skin
7	chr3:195034800-195076800	Weak transcription	Psoas Muscle	Psoas
8	chr3:195040400-195064800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr3:195040400-195066000	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr3:195040400-195076400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr3:195040400-195076600	Weak transcription	Brain Anterior Caudate	brain
12	chr3:195040400-195079400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr3:195040400-195108400	Weak transcription	Colonic Mucosa	Colon
14	chr3:195040600-195111200	Weak transcription	Fetal Brain Male	brain
15	chr3:195040800-195071200	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr3:195040800-195072800	Weak transcription	K562	blood
17	chr3:195040800-195073200	Weak transcription	Pancreas	Pancrea
18	chr3:195040800-195076400	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:195041000-195065400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr3:195041000-195066400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:195041000-195067200	Weak transcription	Brain Substantia Nigra	brain
22	chr3:195041000-195077000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr3:195041000-195131200	Weak transcription	Gastric	stomach
24	chr3:195041200-195077200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:195041400-195064800	Strong transcription	Primary B cells from cord blood	blood
26	chr3:195041400-195076800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr3:195041600-195071600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr3:195041600-195073600	Weak transcription	NHLF	lung
29	chr3:195041600-195077800	Weak transcription	Fetal Brain Female	brain
30	chr3:195045800-195065200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:195048800-195076800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr3:195049600-195106000	Weak transcription	HUVEC	blood vessel
33	chr3:195051800-195073800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr3:195051800-195077000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:195052000-195071400	Weak transcription	HepG2	liver
36	chr3:195052000-195076400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:195052200-195070000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:195052200-195076200	Weak transcription	Colon Smooth Muscle	Colon
39	chr3:195052200-195076800	Weak transcription	Spleen	Spleen
40	chr3:195052200-195077000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr3:195052200-195102800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr3:195052400-195073400	Weak transcription	HSMMtube	muscle
43	chr3:195052400-195076400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr3:195052400-195076800	Weak transcription	Ovary	ovary
45	chr3:195052400-195076800	Weak transcription	Right Ventricle	heart
46	chr3:195052400-195118000	Weak transcription	Stomach Smooth Muscle	stomach
47	chr3:195052600-195077200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr3:195052600-195090400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr3:195053800-195090200	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr3:195056000-195073600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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