Variant report

Variant	rs10941522
Chromosome Location	chr5:40656311-40656312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:40655414..40657452-chr5:40677223..40679951,2	K562	blood:

Variant related genes	Relation type
ENSG00000171522	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10035697	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10038251	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10038367	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10039983	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10040364	0.85[ASN][1000 genomes]
rs10043839	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10043891	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10044538	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10053469	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055624	0.85[ASN][1000 genomes]
rs10056173	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10057182	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10063818	0.85[ASN][1000 genomes]
rs10063864	0.85[ASN][1000 genomes]
rs10065482	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10065874	0.86[ASN][1000 genomes]
rs10065894	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10066459	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10068069	0.88[ASN][1000 genomes]
rs10071870	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10073344	0.85[ASN][1000 genomes]
rs10074117	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10473206	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10473209	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10473210	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10473211	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10473212	0.87[AMR][1000 genomes]
rs10473214	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10473216	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10941521	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11744569	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11744700	0.85[ASN][1000 genomes]
rs11745901	0.83[ASN][1000 genomes]
rs11949581	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11952914	0.85[ASN][1000 genomes]
rs11955037	0.85[ASN][1000 genomes]
rs12188666	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12513529	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1395082	0.85[ASN][1000 genomes]
rs1553578	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1553579	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17238368	0.85[ASN][1000 genomes]
rs17835256	0.89[ASN][1000 genomes]
rs35693860	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45437592	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4599576	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4957333	0.81[AMR][1000 genomes]
rs4957334	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4957336	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4957337	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4957338	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4957339	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4957343	0.89[ASN][1000 genomes]
rs62356460	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62356461	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62358056	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62358796	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62358800	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6860233	0.86[ASN][1000 genomes]
rs6867169	0.85[ASN][1000 genomes]
rs6879155	0.85[ASN][1000 genomes]
rs6879329	0.85[ASN][1000 genomes]
rs6884507	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6892451	0.80[ASN][1000 genomes]
rs72747928	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72747930	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72747940	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7349788	0.85[ASN][1000 genomes]
rs7726047	0.85[ASN][1000 genomes]
rs9292784	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9292785	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880993	chr5:40521648-40682550	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10941522	RPL37	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:40654800-40656400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr5:40655200-40657000	Enhancers	Hela-S3	cervix
3	chr5:40655600-40656400	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr5:40655600-40656400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:40655600-40656600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:40655600-40656800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:40655600-40657000	Enhancers	Primary T cells from cord blood	blood
8	chr5:40655600-40660600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:40655600-40660600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr5:40655600-40669600	Weak transcription	Thymus	Thymus
11	chr5:40656000-40656400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr5:40656200-40656600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr5:40656200-40658200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr5:40656200-40658200	Weak transcription	Dnd41	blood
15	chr5:40656200-40658600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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