Variant report

Variant	rs13150702
Chromosome Location	chr4:122073116-122073117
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:122071769..122073481-chr4:122078376..122080913,2	K562	blood:

Variant related genes	Relation type
ENSG00000050730	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10015340	0.81[EUR][1000 genomes]
rs10446733	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10454795	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10518383	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11098605	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11947841	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13101385	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13102428	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13106084	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13106137	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13107912	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13108214	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13108739	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13109100	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13116723	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13118027	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13118818	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13118913	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13123960	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13124511	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13124522	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13126929	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13128962	0.83[EUR][1000 genomes]
rs13129000	0.83[EUR][1000 genomes]
rs13129293	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13133184	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13133221	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13133584	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13137539	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13138203	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13151913	0.81[EUR][1000 genomes]
rs13152159	0.81[EUR][1000 genomes]
rs13152687	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1511094	0.87[EUR][1000 genomes]
rs17051320	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17051321	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1858291	0.89[EUR][1000 genomes]
rs2068019	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2136942	0.81[EUR][1000 genomes]
rs2136943	0.81[EUR][1000 genomes]
rs2198315	0.81[EUR][1000 genomes]
rs2218959	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28513714	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28530598	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35449703	0.91[ASN][1000 genomes]
rs35971082	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36087391	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3817171	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6534254	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6811411	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6814480	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6820363	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821331	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6828327	0.87[EUR][1000 genomes]
rs6833114	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6835790	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6838000	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6839386	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6839726	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6846458	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6855628	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6856825	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71629498	0.87[ASN][1000 genomes]
rs7684168	0.81[EUR][1000 genomes]
rs867883	0.87[EUR][1000 genomes]
rs9307490	0.81[EUR][1000 genomes]
rs998327	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992960	0.81[EUR][1000 genomes]
rs9993163	0.81[EUR][1000 genomes]
rs9998339	0.81[EUR][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	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1009395	chr4:121841442-122557363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv537235	chr4:121841442-122557363	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv3386870	chr4:121867625-122208448	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv879859	chr4:121892490-122438312	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv879860	chr4:122030864-122126808	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122062000-122074000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr4:122067400-122073400	Enhancers	Osteobl	bone
3	chr4:122070400-122075000	Weak transcription	Fetal Lung	lung
4	chr4:122071000-122073600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:122071000-122073600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:122071200-122074000	Enhancers	Primary T cells from cord blood	blood
7	chr4:122071400-122075000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr4:122071600-122074800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:122071600-122074800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr4:122071600-122075000	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr4:122071800-122074800	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr4:122072000-122073200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr4:122072000-122074800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr4:122072000-122075000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr4:122072400-122074800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr4:122072800-122073600	Enhancers	NHDF-Ad	bronchial
17	chr4:122073000-122074800	Enhancers	Dnd41	blood
18	chr4:122073000-122076400	Enhancers	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links