Variant report

Variant	rs1899036
Chromosome Location	chr2:182161479-182161480
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:125)

rs_ID	r²[population]
rs10175109	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10187534	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10195192	0.84[ASN][1000 genomes]
rs10199252	0.86[EUR][1000 genomes]
rs10206405	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10439303	0.87[ASN][1000 genomes]
rs10497577	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10497579	0.84[ASN][1000 genomes]
rs10930965	0.86[EUR][1000 genomes]
rs10930966	0.86[EUR][1000 genomes]
rs12053408	0.85[ASN][1000 genomes]
rs12616514	0.85[ASN][1000 genomes]
rs12617083	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12618053	0.85[ASN][1000 genomes]
rs12619896	0.85[ASN][1000 genomes]
rs12621204	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12622227	0.84[EUR][1000 genomes]
rs12623045	0.85[ASN][1000 genomes]
rs12623524	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12693274	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13339832	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13339833	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13339865	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13384115	0.86[EUR][1000 genomes]
rs13387919	0.87[EUR][1000 genomes]
rs13390496	0.86[EUR][1000 genomes]
rs13390501	0.87[EUR][1000 genomes]
rs13390598	0.87[EUR][1000 genomes]
rs13393596	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13393709	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13400585	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13400592	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13400891	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13403977	0.87[EUR][1000 genomes]
rs13410482	0.90[ASN][1000 genomes]
rs13410543	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13410843	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13413108	0.87[EUR][1000 genomes]
rs13415095	0.85[ASN][1000 genomes]
rs13416416	0.88[EUR][1000 genomes]
rs13419105	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13426182	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13428910	0.82[ASN][1000 genomes]
rs1371615	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1371622	0.87[ASN][1000 genomes]
rs1371623	0.87[ASN][1000 genomes]
rs1371624	0.85[ASN][1000 genomes]
rs1371625	0.85[ASN][1000 genomes]
rs1440048	0.85[ASN][1000 genomes]
rs1550401	0.85[ASN][1000 genomes]
rs17198661	0.85[ASN][1000 genomes]
rs17270826	0.85[ASN][1000 genomes]
rs17270854	0.85[ASN][1000 genomes]
rs17270861	0.85[ASN][1000 genomes]
rs17365327	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17365362	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17365418	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17456058	0.85[EUR][1000 genomes]
rs17456106	0.88[EUR][1000 genomes]
rs17456148	0.87[EUR][1000 genomes]
rs17456211	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17456294	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2077783	0.87[EUR][1000 genomes]
rs2119148	0.84[EUR][1000 genomes]
rs2218160	0.88[ASN][1000 genomes]
rs2368200	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28716233	0.83[EUR][1000 genomes]
rs3926443	0.84[ASN][1000 genomes]
rs4144311	0.85[ASN][1000 genomes]
rs55646418	0.85[ASN][1000 genomes]
rs56303157	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57063898	0.88[EUR][1000 genomes]
rs57334172	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58997932	0.85[ASN][1000 genomes]
rs59591658	0.87[ASN][1000 genomes]
rs60444729	0.85[ASN][1000 genomes]
rs60689650	0.87[ASN][1000 genomes]
rs60899718	0.85[ASN][1000 genomes]
rs60903476	0.85[ASN][1000 genomes]
rs61235737	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61358146	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62180207	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62180228	0.88[EUR][1000 genomes]
rs62180237	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62180238	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62180239	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62180241	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62180244	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62180245	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62180255	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62180256	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62180257	0.87[ASN][1000 genomes]
rs62180259	0.85[ASN][1000 genomes]
rs62182263	0.85[ASN][1000 genomes]
rs62182264	0.83[ASN][1000 genomes]
rs62182265	0.87[ASN][1000 genomes]
rs6433906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433908	0.81[ASN][1000 genomes]
rs6433909	0.87[ASN][1000 genomes]
rs6704605	0.85[ASN][1000 genomes]
rs6716857	0.85[ASN][1000 genomes]
rs6717513	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6717754	0.86[EUR][1000 genomes]
rs6728366	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6729353	0.86[EUR][1000 genomes]
rs6733437	0.85[ASN][1000 genomes]
rs6743422	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6743583	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6744081	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6757550	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6758852	0.84[ASN][1000 genomes]
rs720453	0.87[EUR][1000 genomes]
rs73036640	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73036646	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7557202	0.85[ASN][1000 genomes]
rs7563015	0.84[ASN][1000 genomes]
rs7564749	0.86[EUR][1000 genomes]
rs7564976	0.86[EUR][1000 genomes]
rs7602997	0.84[EUR][1000 genomes]
rs9288064	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9288065	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs959382	0.85[ASN][1000 genomes]
rs972605	0.86[EUR][1000 genomes]
rs976384	0.87[ASN][1000 genomes]
rs9973857	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][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	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1002647	chr2:182078521-182392273	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536064	chr2:182078521-182392273	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182153000-182164000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr2:182159000-182163800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr2:182160200-182165400	Weak transcription	Fetal Thymus	thymus
4	chr2:182160400-182165400	Weak transcription	Thymus	Thymus
5	chr2:182161400-182163800	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links