Variant report

Variant	rs2792022
Chromosome Location	chr10:93740429-93740430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11186755	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11186768	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1137825	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11592774	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11598321	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11598436	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1229579	1.00[YRI][hapmap]
rs12413858	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12415793	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12416560	1.00[CHB][hapmap];0.98[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12569736	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12571564	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12763600	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12766605	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12771773	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12774295	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12774665	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12777025	0.81[ASN][1000 genomes]
rs12779538	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12780724	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1340421	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1437	1.00[CHB][hapmap];0.98[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1474051	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1581239	0.88[ASN][1000 genomes]
rs1626927	0.88[ASN][1000 genomes]
rs1711842	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1711846	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1711858	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1776209	0.86[CHB][hapmap];0.81[CHD][hapmap];0.86[JPT][hapmap]
rs1776210	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2252204	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676802	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2676808	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2676809	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2676814	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676817	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676819	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676820	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676822	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2676825	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2792018	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2792025	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2797639	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2797647	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2995545	0.90[ASN][1000 genomes]
rs2995546	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34364047	0.90[ASN][1000 genomes]
rs3814639	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3814640	0.95[CHB][hapmap];0.98[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4375360	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4933224	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4933705	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4933706	1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4933707	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7078559	1.00[YRI][hapmap]
rs7087501	1.00[YRI][hapmap]
rs7904126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7909492	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7917105	0.83[ASN][1000 genomes]
rs833366	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs833367	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs833370	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs833372	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs833373	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs833374	0.90[ASN][1000 genomes]
rs833375	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs833378	0.91[ASN][1000 genomes]
rs833384	0.88[ASW][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.91[MEX][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs833385	1.00[YRI][hapmap]
rs855563	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs855702	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051226	chr10:93711296-93915586	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv540745	chr10:93711296-93915586	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1042818	chr10:93715483-93855032	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2792022	TNKS2	cis	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93690800-93742400	Weak transcription	Stomach Mucosa	stomach
2	chr10:93691800-93741400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:93697800-93748800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr10:93699600-93750600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr10:93704800-93807400	Weak transcription	Gastric	stomach
6	chr10:93709000-93771800	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr10:93710000-93750200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr10:93713600-93744400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:93714400-93743800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:93714600-93768000	Weak transcription	Right Ventricle	heart
11	chr10:93715400-93741400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr10:93718400-93774000	Weak transcription	Spleen	Spleen
13	chr10:93719400-93761000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr10:93720000-93741400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr10:93720000-93757400	Weak transcription	Small Intestine	intestine
16	chr10:93720200-93741400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr10:93720400-93741800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr10:93720400-93757400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:93720600-93742600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr10:93720600-93742800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr10:93721200-93741200	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr10:93721200-93742000	Weak transcription	Fetal Kidney	kidney
23	chr10:93721400-93742000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr10:93721600-93741600	Weak transcription	Brain Anterior Caudate	brain
25	chr10:93721600-93743200	Weak transcription	Lung	lung
26	chr10:93722200-93741400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr10:93722400-93741400	Weak transcription	Thymus	Thymus
28	chr10:93723800-93743000	Weak transcription	Aorta	Aorta
29	chr10:93723800-93786600	Weak transcription	Colonic Mucosa	Colon
30	chr10:93724200-93748200	Weak transcription	Psoas Muscle	Psoas
31	chr10:93724600-93741800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr10:93726000-93741800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr10:93726400-93741800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr10:93726600-93742000	Weak transcription	Brain Germinal Matrix	brain
35	chr10:93728000-93757400	Weak transcription	Fetal Brain Male	brain
36	chr10:93728200-93741200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr10:93728200-93741200	Weak transcription	Rectal Smooth Muscle	rectum
38	chr10:93728200-93741800	Weak transcription	Brain Substantia Nigra	brain
39	chr10:93728400-93741800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr10:93728600-93741600	Weak transcription	A549	lung
41	chr10:93728600-93741800	Weak transcription	Brain Angular Gyrus	brain
42	chr10:93728600-93741800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr10:93728600-93751600	Weak transcription	K562	blood
44	chr10:93728800-93741400	Weak transcription	Fetal Muscle Leg	muscle
45	chr10:93728800-93741800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr10:93729800-93765600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:93730000-93743000	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr10:93730200-93742400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr10:93730200-93747000	Weak transcription	Fetal Stomach	stomach
50	chr10:93730400-93750200	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links