Variant report

Variant	rs28451271
Chromosome Location	chr4:151582753-151582754
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10000491	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10000655	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10025007	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10025414	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10155442	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10857247	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11099766	0.82[EUR][1000 genomes]
rs11099773	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11099774	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11931175	0.92[EUR][1000 genomes]
rs12108435	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12499862	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12508892	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12642528	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13103943	0.84[EUR][1000 genomes]
rs13111441	0.87[EUR][1000 genomes]
rs13144332	0.87[EUR][1000 genomes]
rs1504781	0.87[EUR][1000 genomes]
rs1504784	0.97[EUR][1000 genomes]
rs1532822	0.92[EUR][1000 genomes]
rs2884894	0.81[EUR][1000 genomes]
rs4235250	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4269161	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4270570	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4289432	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4311291	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4327465	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4328896	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4330340	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4355367	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4358377	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4376124	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4396972	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4401437	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4417951	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4450905	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4476581	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4533751	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4568218	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4604037	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4619872	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4619873	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4696186	0.92[EUR][1000 genomes]
rs4696214	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4696537	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4696629	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6535743	0.80[AMR][1000 genomes]
rs6535744	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs68016242	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6818709	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6825990	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6826248	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6832498	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6839548	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6846154	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6847725	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6851587	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6852493	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6852703	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6855667	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6858267	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7671045	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7674989	0.87[EUR][1000 genomes]
rs7686220	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7692615	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs905767	0.87[EUR][1000 genomes]
rs9790393	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9995388	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9995612	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9997018	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880256	chr4:151126725-151751369	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv817540	chr4:151228965-151858609	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv869051	chr4:151347901-151737781	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1032070	chr4:151514664-151775259	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv880261	chr4:151521933-151588483	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv830113	chr4:151538184-151691942	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
8	nsv1029861	chr4:151556384-151720601	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv3429899	chr4:151579652-151583200	ZNF genes & repeats Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3440371	chr4:151580127-151582875	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151487200-151655000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:151533400-151596200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:151554800-151585200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:151555800-151585600	Weak transcription	Primary B cells from cord blood	blood
5	chr4:151571200-151601600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr4:151571200-151604600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr4:151573200-151583800	Weak transcription	Lung	lung
8	chr4:151574800-151601200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:151576600-151585600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:151577600-151637000	Weak transcription	Primary T cells from cord blood	blood
11	chr4:151578600-151589600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr4:151579400-151604400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr4:151581000-151584000	Weak transcription	Fetal Stomach	stomach
14	chr4:151582200-151583800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:151582200-151642800	Weak transcription	Left Ventricle	heart
16	chr4:151582400-151583000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:151582400-151583200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:151582400-151583200	Enhancers	NHEK	skin
19	chr4:151582600-151583400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:151582600-151583400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:151582600-151595800	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links