Variant report

Variant	rs10241036
Chromosome Location	chr7:125036661-125036662
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10085610	0.98[EUR][1000 genomes]
rs10085871	0.99[EUR][1000 genomes]
rs10085895	0.99[EUR][1000 genomes]
rs10500110	0.93[EUR][1000 genomes]
rs10808221	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10954070	0.96[EUR][1000 genomes]
rs10954072	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10954073	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11763577	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11766248	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11770231	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11770385	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11770393	1.00[ASN][1000 genomes]
rs11974022	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12673529	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13225573	0.81[EUR][1000 genomes]
rs1344654	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1346357	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1346358	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1358148	0.94[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.94[TSI][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1427569	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1427570	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1427584	0.95[EUR][1000 genomes]
rs17148196	0.81[CHD][hapmap];0.88[JPT][hapmap]
rs17148321	0.93[EUR][1000 genomes]
rs2042819	0.97[EUR][1000 genomes]
rs2042821	0.99[EUR][1000 genomes]
rs4262272	0.95[EUR][1000 genomes]
rs4268072	1.00[CEU][hapmap];0.98[GIH][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.95[EUR][1000 genomes]
rs4452732	0.93[EUR][1000 genomes]
rs4496892	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs4537243	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57140942	0.95[EUR][1000 genomes]
rs60052046	0.93[EUR][1000 genomes]
rs62479865	0.95[EUR][1000 genomes]
rs6467004	0.95[EUR][1000 genomes]
rs6467005	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6467006	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6467009	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6945040	0.95[EUR][1000 genomes]
rs6945564	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6951568	0.96[EUR][1000 genomes]
rs6952136	0.95[EUR][1000 genomes]
rs6952222	0.96[EUR][1000 genomes]
rs6956746	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6957878	0.96[EUR][1000 genomes]
rs6961673	0.97[EUR][1000 genomes]
rs6961775	0.99[EUR][1000 genomes]
rs6961868	0.99[EUR][1000 genomes]
rs6961942	0.98[EUR][1000 genomes]
rs6961969	0.99[EUR][1000 genomes]
rs6962494	0.99[EUR][1000 genomes]
rs6962726	0.93[EUR][1000 genomes]
rs6965116	0.96[EUR][1000 genomes]
rs6966097	0.99[EUR][1000 genomes]
rs6966372	0.99[EUR][1000 genomes]
rs6966447	0.99[EUR][1000 genomes]
rs6972166	0.96[EUR][1000 genomes]
rs6976619	0.96[EUR][1000 genomes]
rs6979984	0.95[EUR][1000 genomes]
rs7780175	0.95[EUR][1000 genomes]
rs7780500	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7780578	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7783813	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7784326	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7784402	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7790843	0.93[EUR][1000 genomes]
rs7791113	0.93[EUR][1000 genomes]
rs7804579	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7807227	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs934026	0.96[EUR][1000 genomes]
rs934027	0.94[EUR][1000 genomes]
rs934028	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422188	chr7:124782873-125254203	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	esv2761087	chr7:124823624-125429662	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv889140	chr7:124921028-125042024	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv464709	chr7:124921028-125068580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv608345	chr7:124921028-125068580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv889141	chr7:124935779-125072969	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv889142	chr7:124958806-125068580	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1028369	chr7:124967804-125508233	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv948720	chr7:124970772-125783434	Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv889143	chr7:124977736-125042024	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv889144	chr7:124977736-125068580	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv889145	chr7:124977736-125231999	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv889146	chr7:124996787-125083020	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1023903	chr7:125027662-125057454	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10241036	TAS2R16	cis	parietal	SCAN
rs10241036	LOC407835	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:125035800-125039200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:125035800-125039800	Enhancers	Primary hematopoietic stem cells	blood
3	chr7:125036200-125038600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr7:125036400-125037600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:125036400-125037800	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links