Variant report

Variant	rs73404729
Chromosome Location	chr15:42807997-42807998
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1044866	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11541527	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16973349	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs36090286	0.85[AFR][1000 genomes]
rs5009460	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57249373	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57349778	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs58122107	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs58562675	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58952814	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59058205	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59091063	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60060355	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60168929	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60606292	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60697170	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60839827	1.00[AMR][1000 genomes]
rs61368952	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61474811	0.85[AMR][1000 genomes]
rs6493048	0.92[AFR][1000 genomes]
rs6493049	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6493050	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7166143	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7166633	0.87[AMR][1000 genomes]
rs7172064	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7172955	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7173155	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7175059	0.87[AMR][1000 genomes]
rs7178822	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7181938	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73402762	0.85[AMR][1000 genomes]
rs73402776	0.85[AMR][1000 genomes]
rs73402796	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73404708	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404711	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404725	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404744	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404746	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404754	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73404758	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404768	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404774	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404775	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404793	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73404797	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406503	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406505	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406509	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406526	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406531	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406544	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406553	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73406557	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs768118	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8023948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8027207	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8031383	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8031883	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8033555	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8033810	1.00[AMR][1000 genomes]
rs8034001	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8035877	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8036927	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8037277	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8040624	0.91[AFR][1000 genomes];1.00[AMR][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	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3334708	chr15:42664344-42827738	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv528725	chr15:42755555-43104406	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42788400-42808000	Weak transcription	Esophagus	oesophagus
2	chr15:42790800-42809800	Weak transcription	Spleen	Spleen
3	chr15:42790800-42810000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr15:42790800-42821400	Weak transcription	Right Ventricle	heart
5	chr15:42791200-42809800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:42793000-42809800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:42793000-42835600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:42793800-42837200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr15:42797400-42839800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:42797600-42822200	Weak transcription	Small Intestine	intestine
11	chr15:42797600-42839400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr15:42798600-42808400	Weak transcription	Gastric	stomach
13	chr15:42799200-42839400	Weak transcription	Stomach Mucosa	stomach
14	chr15:42801000-42809400	Weak transcription	Fetal Lung	lung
15	chr15:42802200-42812000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr15:42802400-42839200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:42802600-42811800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr15:42802600-42817400	Strong transcription	Primary B cells from peripheral blood	blood
19	chr15:42802800-42817200	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr15:42803000-42810600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr15:42803200-42808000	Weak transcription	Psoas Muscle	Psoas
22	chr15:42803200-42809000	Weak transcription	NHLF	lung
23	chr15:42803200-42837200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:42803400-42808200	Weak transcription	Aorta	Aorta
25	chr15:42803600-42839400	Weak transcription	A549	lung
26	chr15:42803800-42808600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr15:42803800-42817600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr15:42804000-42810600	Strong transcription	NHEK	skin
29	chr15:42804000-42826800	Strong transcription	HUVEC	blood vessel
30	chr15:42804400-42814400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr15:42804600-42836400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr15:42804800-42808200	Strong transcription	Primary B cells from cord blood	blood
33	chr15:42804800-42808600	Strong transcription	Osteobl	bone
34	chr15:42804800-42812200	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr15:42804800-42812400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr15:42804800-42814600	Strong transcription	Primary T cells from cord blood	blood
37	chr15:42804800-42817200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr15:42804800-42817400	Strong transcription	Adipose Nuclei	Adipose
39	chr15:42804800-42818000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr15:42804800-42818000	Strong transcription	Fetal Intestine Large	intestine
41	chr15:42804800-42825400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr15:42804800-42828800	Strong transcription	Placenta	Placenta
43	chr15:42804800-42836400	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr15:42804800-42836400	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr15:42805000-42811400	Strong transcription	HSMM	muscle
46	chr15:42805000-42812200	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr15:42805000-42814400	Strong transcription	Fetal Thymus	thymus
48	chr15:42805000-42814600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr15:42805000-42818400	Strong transcription	Rectal Mucosa Donor 29	rectum
50	chr15:42805000-42818800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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