Variant report

Variant	rs73024645
Chromosome Location	chr19:21290744-21290745
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10413569	0.87[EUR][1000 genomes]
rs10413841	0.84[EUR][1000 genomes]
rs10416447	0.87[EUR][1000 genomes]
rs10425841	0.95[EUR][1000 genomes]
rs11085427	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11085429	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12052091	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12150909	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12151107	0.88[EUR][1000 genomes]
rs17618418	0.85[EUR][1000 genomes]
rs2358793	0.93[EUR][1000 genomes]
rs3919641	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3937493	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4580323	0.88[EUR][1000 genomes]
rs61733856	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66693308	0.98[EUR][1000 genomes]
rs73012909	0.85[EUR][1000 genomes]
rs73012916	0.88[EUR][1000 genomes]
rs73012919	0.88[EUR][1000 genomes]
rs73012925	0.88[EUR][1000 genomes]
rs73012931	0.88[EUR][1000 genomes]
rs73012943	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73014828	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73014838	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73014844	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73014852	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73014854	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73014855	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73014863	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73014868	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73018961	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73018974	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73018975	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73018978	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73019002	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020605	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020608	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020616	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020624	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020625	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020628	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020630	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020631	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020636	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020644	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020654	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73020661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73022623	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73022624	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73022630	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73022634	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73022639	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73022640	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73022648	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73022667	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024637	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024648	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024655	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024657	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024662	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024665	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73024668	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024670	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024671	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024674	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024675	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024685	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73024688	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73026655	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73026661	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73026662	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73026693	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv817536	chr19:21041855-21348237	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv1850387	chr19:21109758-21294264	Active TSS ZNF genes & repeats Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv960811	chr19:21200306-21371757	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	esv3399352	chr19:21232738-21423323	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv911412	chr19:21233388-21297358	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1065384	chr19:21249321-21350698	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv911413	chr19:21263518-21347598	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	esv3319019	chr19:21268262-21336383	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	esv3319020	chr19:21268262-21336383	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	esv7695	chr19:21268276-21328430	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	esv5909	chr19:21272333-21334753	Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
13	esv3420290	chr19:21272477-21336432	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	esv3391713	chr19:21272485-21334631	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
15	esv5243	chr19:21272548-21334670	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
16	esv7204	chr19:21274198-21336396	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
17	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
18	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21265600-21295800	Weak transcription	Small Intestine	intestine
2	chr19:21265600-21300000	Weak transcription	Brain Angular Gyrus	brain
3	chr19:21265600-21305200	Weak transcription	Psoas Muscle	Psoas
4	chr19:21265800-21297200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr19:21265800-21297200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr19:21265800-21299600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr19:21265800-21299800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:21265800-21302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:21265800-21302800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr19:21265800-21303000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr19:21266000-21290800	Weak transcription	Brain Anterior Caudate	brain
12	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr19:21266000-21292600	Weak transcription	Fetal Kidney	kidney
15	chr19:21266000-21297400	Weak transcription	HUVEC	blood vessel
16	chr19:21266200-21292400	Weak transcription	Primary T cells from cord blood	blood
17	chr19:21266200-21296600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr19:21266200-21301600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr19:21266800-21292600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr19:21267000-21292800	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr19:21267200-21295800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:21271200-21296000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr19:21274400-21291200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr19:21275400-21292800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr19:21275400-21294200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr19:21275400-21297200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr19:21275400-21301400	Weak transcription	Fetal Brain Male	brain
28	chr19:21275400-21304600	Weak transcription	Stomach Smooth Muscle	stomach
29	chr19:21275600-21290800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr19:21275600-21293000	Weak transcription	Primary B cells from cord blood	blood
31	chr19:21275600-21299000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr19:21276200-21293000	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr19:21276400-21293000	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr19:21278200-21292600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:21280000-21297400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr19:21281600-21291600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr19:21281800-21300000	Weak transcription	HMEC	breast
38	chr19:21282400-21291200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:21282600-21292400	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr19:21282800-21293600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr19:21283200-21297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:21283600-21292800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr19:21284200-21302600	Weak transcription	Brain Substantia Nigra	brain
44	chr19:21284600-21296600	Weak transcription	K562	blood
45	chr19:21284600-21306800	Weak transcription	Left Ventricle	heart
46	chr19:21284800-21291600	Weak transcription	Osteobl	bone
47	chr19:21285000-21290800	Weak transcription	HSMMtube	muscle
48	chr19:21285000-21291000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:21285000-21291000	Weak transcription	NHEK	skin
50	chr19:21285000-21297200	Weak transcription	HepG2	liver

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