Variant report

Variant	rs10759145
Chromosome Location	chr9:108606135-108606136
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 123 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs10114077	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10116066	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10117187	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10118661	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10121208	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10122308	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs10156569	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10156571	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10217508	0.80[EUR][1000 genomes]
rs10441744	0.80[EUR][1000 genomes]
rs10512340	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10512341	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10739213	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10759128	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10759132	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10759133	0.86[CHB][hapmap];0.80[JPT][hapmap]
rs10759135	0.82[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10759143	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10759144	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10759146	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10816294	0.86[JPT][hapmap]
rs10816295	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs10816296	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs10816297	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs10816298	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs10816299	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10816300	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs10816302	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10816310	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs10816313	0.91[CHB][hapmap]
rs10816314	0.80[EUR][1000 genomes]
rs10816319	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10816324	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10816330	0.80[EUR][1000 genomes]
rs10816331	0.80[EUR][1000 genomes]
rs10816337	0.80[EUR][1000 genomes]
rs10816345	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10816346	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10816347	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10978196	0.86[JPT][hapmap]
rs10978202	0.86[JPT][hapmap]
rs10978203	0.86[JPT][hapmap]
rs10978220	0.82[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs10978226	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10978230	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10978235	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs10978239	0.82[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10978240	0.82[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10978241	0.90[CHB][hapmap]
rs10978251	0.80[EUR][1000 genomes]
rs10978252	0.80[EUR][1000 genomes]
rs10978257	0.80[EUR][1000 genomes]
rs10978265	0.80[EUR][1000 genomes]
rs10978300	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10978301	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10978302	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10978303	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10978306	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11506857	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11506858	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12338851	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs12344129	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs12345343	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs12346407	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12347783	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs12684672	0.84[CHB][hapmap];0.81[JPT][hapmap]
rs13286237	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs1509424	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1979992	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs1979993	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2175121	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2175122	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2271246	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs2417621	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28534814	0.81[ASN][1000 genomes]
rs2900400	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3010415	0.87[CHB][hapmap];0.81[ASN][1000 genomes]
rs3010964	0.89[ASN][1000 genomes]
rs3105991	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs3817141	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs4292753	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4563949	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6477455	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs6477460	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs6477462	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs6477463	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs6477469	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6477470	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6477472	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6477473	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6477474	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7020523	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7024111	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7024357	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7024988	0.83[CHB][hapmap]
rs7026814	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs7026968	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs7028906	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7030236	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7031360	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs7031431	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7043222	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7046212	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7046293	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7047678	0.86[JPT][hapmap]
rs7861268	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7862565	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7865672	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs7872125	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7873663	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs7875434	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs872245	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs872246	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9777628	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs9969715	0.87[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv893694	chr9:108486533-108854018	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1041073	chr9:108535813-108731343	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv508558	chr9:108536115-108611087	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	n/a
5	nsv1036849	chr9:108582944-108651205	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1052684	chr9:108582944-108730280	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv615140	chr9:108592589-108725567	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv831679	chr9:108603112-108785347	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10759145	TMEM38B	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108598400-108615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:108604800-108609400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links