Variant report

Variant	rs7901941
Chromosome Location	chr10:28473692-28473693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10508736	0.87[ASN][1000 genomes]
rs10740785	0.87[ASN][1000 genomes]
rs10740786	0.87[ASN][1000 genomes]
rs10763646	0.87[ASN][1000 genomes]
rs10763647	0.87[ASN][1000 genomes]
rs10763648	0.87[ASN][1000 genomes]
rs10763649	0.87[ASN][1000 genomes]
rs10763650	0.87[ASN][1000 genomes]
rs10826414	0.87[ASN][1000 genomes]
rs10826415	0.86[ASN][1000 genomes]
rs10826417	0.87[ASN][1000 genomes]
rs10826418	0.87[ASN][1000 genomes]
rs10826419	0.87[ASN][1000 genomes]
rs10826421	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10826422	0.87[ASN][1000 genomes]
rs10826424	0.85[ASN][1000 genomes]
rs11006914	0.84[ASN][1000 genomes]
rs11006915	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006917	0.87[ASN][1000 genomes]
rs12049636	0.87[ASN][1000 genomes]
rs12221232	0.87[ASN][1000 genomes]
rs12248472	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12251587	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12255686	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12357915	0.86[ASN][1000 genomes]
rs17831690	0.86[ASN][1000 genomes]
rs1824172	0.87[ASN][1000 genomes]
rs1824173	0.86[ASN][1000 genomes]
rs1937807	0.86[ASN][1000 genomes]
rs1937808	0.86[ASN][1000 genomes]
rs1937809	0.86[ASN][1000 genomes]
rs2607539	0.87[ASN][1000 genomes]
rs2607542	0.87[ASN][1000 genomes]
rs2607543	0.87[ASN][1000 genomes]
rs2607544	0.87[ASN][1000 genomes]
rs2607545	0.86[ASN][1000 genomes]
rs2607546	0.86[ASN][1000 genomes]
rs2801833	0.86[ASN][1000 genomes]
rs2801834	0.84[ASN][1000 genomes]
rs2801835	0.87[ASN][1000 genomes]
rs2985521	0.86[ASN][1000 genomes]
rs2985535	0.87[ASN][1000 genomes]
rs2997210	0.87[ASN][1000 genomes]
rs3847382	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3901407	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3905706	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4018718	0.87[ASN][1000 genomes]
rs4568902	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7067826	0.87[ASN][1000 genomes]
rs7068687	0.83[ASN][1000 genomes]
rs7088552	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72631847	0.87[ASN][1000 genomes]
rs7893311	0.87[ASN][1000 genomes]
rs7915273	0.87[ASN][1000 genomes]
rs7922685	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1042524	chr10:28290149-28506812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831816	chr10:28304698-28493635	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv831817	chr10:28369836-28539930	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
9	esv3375324	chr10:28472221-28475144	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28449800-28497000	Weak transcription	Fetal Intestine Small	intestine
2	chr10:28467600-28485400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr10:28467600-28491800	Weak transcription	Psoas Muscle	Psoas
4	chr10:28467600-28525600	Weak transcription	Aorta	Aorta
5	chr10:28467800-28495200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr10:28468200-28484600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr10:28469800-28491000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr10:28470000-28485600	Weak transcription	Primary T cells from cord blood	blood
9	chr10:28471000-28476200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:28471600-28474400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:28471600-28475600	Weak transcription	Fetal Heart	heart

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