Variant report

Variant	rs73254548
Chromosome Location	chr14:31171727-31171728
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs17348231	0.84[EUR][1000 genomes]
rs17348259	1.00[EUR][1000 genomes]
rs17362475	1.00[EUR][1000 genomes]
rs17363198	1.00[EUR][1000 genomes]
rs17433265	1.00[EUR][1000 genomes]
rs1884582	1.00[EUR][1000 genomes]
rs28483238	1.00[EUR][1000 genomes]
rs45531233	1.00[EUR][1000 genomes]
rs57216699	0.97[AFR][1000 genomes]
rs57549139	0.83[AFR][1000 genomes]
rs57618174	0.83[AFR][1000 genomes]
rs57677010	0.83[AFR][1000 genomes]
rs58653311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60350877	0.83[AFR][1000 genomes]
rs60353606	0.83[AFR][1000 genomes]
rs60362029	0.83[AFR][1000 genomes]
rs60727186	1.00[AFR][1000 genomes]
rs7157286	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73251132	0.83[AFR][1000 genomes]
rs73251134	0.83[AFR][1000 genomes]
rs73251145	0.83[AFR][1000 genomes]
rs73251146	0.83[AFR][1000 genomes]
rs73251151	0.97[AFR][1000 genomes]
rs73251156	0.97[AFR][1000 genomes]
rs73251167	0.90[AFR][1000 genomes]
rs73251169	0.97[AFR][1000 genomes]
rs73251177	0.97[AFR][1000 genomes]
rs73251179	0.97[AFR][1000 genomes]
rs73251181	0.97[AFR][1000 genomes]
rs73251184	0.97[AFR][1000 genomes]
rs73251188	0.97[AFR][1000 genomes]
rs73251199	1.00[AFR][1000 genomes]
rs73253017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254552	1.00[AFR][1000 genomes]
rs73254553	1.00[AFR][1000 genomes]
rs73254554	1.00[AFR][1000 genomes]
rs73254555	1.00[AFR][1000 genomes]
rs73254556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254558	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73254562	1.00[EUR][1000 genomes]
rs73254565	1.00[AFR][1000 genomes]
rs73254568	1.00[AFR][1000 genomes]
rs73254580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254583	1.00[AFR][1000 genomes]
rs73254586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254588	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73254589	1.00[AFR][1000 genomes]
rs73255979	0.83[AFR][1000 genomes]
rs73255992	0.83[AFR][1000 genomes]
rs73258111	0.83[AFR][1000 genomes]
rs73258118	0.83[AFR][1000 genomes]
rs73258119	0.83[AFR][1000 genomes]
rs73264309	0.83[AFR][1000 genomes]
rs73264311	0.83[AFR][1000 genomes]
rs73264321	0.83[AFR][1000 genomes]
rs73264329	0.83[AFR][1000 genomes]
rs73264330	0.83[AFR][1000 genomes]
rs73264333	0.83[AFR][1000 genomes]
rs73264341	0.83[AFR][1000 genomes]
rs73264346	0.83[AFR][1000 genomes]
rs73264352	0.83[AFR][1000 genomes]
rs73264362	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564169	chr14:30819087-31541494	Strong transcription Genic enhancers ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1036419	chr14:30969616-31224226	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv901581	chr14:30978745-31585289	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31113800-31205400	Weak transcription	Fetal Brain Male	brain
2	chr14:31122800-31205200	Weak transcription	Brain Angular Gyrus	brain
3	chr14:31123000-31212000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr14:31123400-31216400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr14:31133800-31197400	Weak transcription	Aorta	Aorta
6	chr14:31153600-31174400	Weak transcription	NHDF-Ad	bronchial
7	chr14:31153600-31198800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:31153800-31187400	Weak transcription	Fetal Brain Female	brain
9	chr14:31160000-31206600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:31160000-31207200	Weak transcription	Right Ventricle	heart
11	chr14:31160200-31172800	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr14:31160200-31176000	Strong transcription	HSMM	muscle
13	chr14:31160200-31178800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:31160400-31205000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr14:31160600-31192400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr14:31160800-31197400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr14:31160800-31198600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:31160800-31206200	Weak transcription	Small Intestine	intestine
19	chr14:31161000-31178600	Weak transcription	Stomach Mucosa	stomach
20	chr14:31161000-31180800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr14:31161000-31195600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:31161000-31195800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr14:31161600-31197000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr14:31161800-31199000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:31162000-31181000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr14:31162000-31192000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr14:31162200-31192000	Weak transcription	A549	lung
28	chr14:31162200-31199200	Strong transcription	HepG2	liver
29	chr14:31162400-31204000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr14:31162600-31194000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr14:31162800-31183200	Weak transcription	Fetal Heart	heart
32	chr14:31163400-31179000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:31163600-31172000	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr14:31163600-31179400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:31163600-31180000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:31163800-31171800	Strong transcription	Primary hematopoietic stem cells	blood
37	chr14:31163800-31172000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr14:31163800-31172400	Strong transcription	Adipose Nuclei	Adipose
39	chr14:31163800-31172600	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr14:31164000-31171800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr14:31164000-31172000	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr14:31164000-31172800	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr14:31164000-31172800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr14:31164200-31172800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:31164400-31171800	Strong transcription	Primary B cells from peripheral blood	blood
46	chr14:31164400-31195800	Weak transcription	Brain Substantia Nigra	brain
47	chr14:31164600-31171800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr14:31165000-31208200	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr14:31166000-31204200	Weak transcription	Colonic Mucosa	Colon
50	chr14:31166000-31205600	Weak transcription	Thymus	Thymus

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