Variant report

Variant	rs4744139
Chromosome Location	chr9:95301397-95301398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10114912	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10114932	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10115290	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10116241	0.81[ASN][1000 genomes]
rs10117627	0.83[EUR][1000 genomes]
rs10117680	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10118107	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10118939	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10120329	0.93[ASN][1000 genomes]
rs10123738	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10125450	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10429459	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10514815	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1075397	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10761158	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10761163	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10761164	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10820986	1.00[ASN][1000 genomes]
rs10820988	1.00[ASN][1000 genomes]
rs10820989	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10820990	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10992347	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10992365	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10992366	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10992375	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11789163	0.81[ASN][1000 genomes]
rs11795122	0.82[ASN][1000 genomes]
rs12335553	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12338938	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12343820	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13301492	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13301652	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1535754	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1924243	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1924244	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2026585	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2094281	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2104533	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2296666	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2296667	0.82[ASN][1000 genomes]
rs2895219	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3739606	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3780347	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3927488	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4302908	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4743873	0.80[AMR][1000 genomes]
rs4743874	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4744133	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4744135	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4744136	0.82[ASN][1000 genomes]
rs4744137	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4744138	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6479423	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7029939	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7031567	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs747628	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs747629	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7847534	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7849788	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7849927	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7852510	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7860774	0.81[EUR][1000 genomes]
rs7860786	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7863049	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7864575	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7864630	0.82[ASN][1000 genomes]
rs7865019	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7869742	0.82[ASN][1000 genomes]
rs7872610	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7872644	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7873390	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs927865	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9299405	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs968040	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs987553	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs987554	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv893573	chr9:94974188-95355719	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1047337	chr9:95105638-95347484	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1052846	chr9:95291909-95366109	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4744139	CENPP	cis	Esophagus Muscularis	GTEx

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95296000-95301800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:95297400-95304600	Weak transcription	Left Ventricle	heart
3	chr9:95298800-95301400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr9:95299000-95301400	Enhancers	Osteobl	bone
5	chr9:95299000-95301600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:95299200-95301400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:95299200-95301400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:95299400-95304200	Weak transcription	Ovary	ovary
9	chr9:95299800-95301400	Enhancers	NHDF-Ad	bronchial
10	chr9:95299800-95301600	Enhancers	HSMM	muscle
11	chr9:95300000-95301400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr9:95300000-95301600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:95300200-95301400	Enhancers	HSMMtube	muscle
14	chr9:95300400-95304800	Weak transcription	Fetal Intestine Small	intestine
15	chr9:95300600-95301400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr9:95300600-95301600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr9:95300800-95302200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:95301000-95301600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr9:95301000-95302000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:95301000-95302000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:95301000-95302000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr9:95301000-95302200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr9:95301200-95301400	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links