Variant report

Variant	rs62175367
Chromosome Location	chr2:179922840-179922841
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10497530	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497531	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497532	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11883598	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11883599	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11883748	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11885227	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11885400	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11885450	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11886627	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11887988	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888041	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11890988	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11891599	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11891608	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11891654	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11892227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11893153	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11893315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11895391	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11896002	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11896686	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897059	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11899563	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11901386	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11901918	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11902355	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11903793	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12467652	0.97[EUR][1000 genomes]
rs12474600	0.95[EUR][1000 genomes]
rs13009130	0.85[AMR][1000 genomes]
rs13032202	0.85[AMR][1000 genomes]
rs16866624	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17362972	0.95[EUR][1000 genomes]
rs17363006	0.99[EUR][1000 genomes]
rs17363057	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1875779	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1875782	0.95[EUR][1000 genomes]
rs34190485	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35465824	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35888089	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35901501	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs35979436	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36098953	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4435492	0.95[EUR][1000 genomes]
rs4893864	0.93[EUR][1000 genomes]
rs4991006	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61397643	0.97[EUR][1000 genomes]
rs62175366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175401	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175402	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175403	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175411	0.91[EUR][1000 genomes]
rs62175413	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs62175419	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62175420	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175421	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175422	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175444	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62175990	0.95[EUR][1000 genomes]
rs62175993	0.95[EUR][1000 genomes]
rs62175994	0.95[EUR][1000 genomes]
rs62175995	0.95[EUR][1000 genomes]
rs62176021	0.95[EUR][1000 genomes]
rs62176023	0.99[EUR][1000 genomes]
rs62176024	0.99[EUR][1000 genomes]
rs62176026	0.99[EUR][1000 genomes]
rs62176027	0.99[EUR][1000 genomes]
rs62176028	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs62176030	0.81[EUR][1000 genomes]
rs6433747	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433748	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433749	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433750	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433751	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433752	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6709090	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716599	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716728	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6731564	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6731566	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6734597	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7574853	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7575047	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7578521	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7578961	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7579263	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7582862	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7588765	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7596842	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7601179	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7605060	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7609150	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949133	chr2:179711376-180124327	Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv875457	chr2:179775893-179966804	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875458	chr2:179780624-179966804	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv875464	chr2:179843612-179939493	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv875465	chr2:179843612-179966804	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv508184	chr2:179896384-179965419	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179915200-179923000	Weak transcription	Right Atrium	heart
2	chr2:179916400-179923000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:179918600-179923000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:179921800-179923200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:179921800-179924400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:179922000-179923000	Enhancers	HSMMtube	muscle
7	chr2:179922000-179923600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr2:179922000-179924200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:179922200-179923200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr2:179922200-179923200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:179922200-179923400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:179922200-179924000	Enhancers	HSMM	muscle
13	chr2:179922200-179924600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:179922400-179923600	Enhancers	Primary hematopoietic stem cells	blood
15	chr2:179922400-179923600	Enhancers	Fetal Muscle Leg	muscle
16	chr2:179922400-179924600	Enhancers	Fetal Heart	heart
17	chr2:179922600-179923400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr2:179922600-179923400	Enhancers	GM12878-XiMat	blood
19	chr2:179922600-179923600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:179922600-179923600	Enhancers	Fetal Lung	lung
21	chr2:179922600-179923600	Enhancers	Placenta	Placenta
22	chr2:179922600-179923600	Enhancers	Left Ventricle	heart
23	chr2:179922600-179923600	Enhancers	Right Ventricle	heart
24	chr2:179922600-179924400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr2:179922600-179924400	Enhancers	Primary B cells from peripheral blood	blood
26	chr2:179922600-179924800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr2:179922800-179923200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:179922800-179923400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:179922800-179923400	Enhancers	A549	lung
30	chr2:179922800-179923600	Enhancers	Fetal Stomach	stomach
31	chr2:179922800-179923600	Enhancers	Gastric	stomach
32	chr2:179922800-179923600	Enhancers	Ovary	ovary
33	chr2:179922800-179923600	Enhancers	Stomach Smooth Muscle	stomach
34	chr2:179922800-179923800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr2:179922800-179924000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:179922800-179924000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:179922800-179924200	Enhancers	Adipose Nuclei	Adipose
38	chr2:179922800-179924400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:179922800-179924600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:179922800-179924800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:179922800-179925200	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links