Variant report

Variant	rs1884406
Chromosome Location	chr14:37873514-37873515
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:37868487..37870431-chr14:37872042..37874988,2	K562	blood:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10129341	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10132634	0.90[AFR][1000 genomes]
rs10132652	1.00[AFR][1000 genomes]
rs10132727	1.00[ASW][hapmap];0.82[AFR][1000 genomes]
rs10134469	1.00[ASW][hapmap]
rs10135014	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10136240	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10137554	0.89[YRI][hapmap];0.90[AFR][1000 genomes]
rs10141822	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10143648	1.00[ASW][hapmap]
rs10144237	0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10148472	1.00[ASW][hapmap]
rs1014880	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs10150559	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[MKK][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs10782385	1.00[ASW][hapmap]
rs10782386	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12434053	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12437318	1.00[AFR][1000 genomes]
rs12717263	0.90[AFR][1000 genomes]
rs1474887	0.89[YRI][hapmap]
rs1474888	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1950518	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1950530	1.00[AMR][1000 genomes]
rs1950535	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1955931	1.00[ASW][hapmap]
rs1955932	0.97[AFR][1000 genomes]
rs1955933	0.97[AFR][1000 genomes]
rs1955941	1.00[ASW][hapmap]
rs1955947	0.89[YRI][hapmap];1.00[AMR][1000 genomes]
rs1955948	1.00[ASW][hapmap]
rs1955953	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1955954	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1955956	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2103893	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2180252	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2180253	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2207861	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2207863	0.97[AFR][1000 genomes]
rs2224155	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2224344	1.00[ASW][hapmap]
rs2899858	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs4522332	1.00[AFR][1000 genomes]
rs4898593	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs4900834	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6571808	0.97[AFR][1000 genomes]
rs6571809	0.93[AFR][1000 genomes]
rs7142072	1.00[ASW][hapmap];0.86[LWK][hapmap];0.89[YRI][hapmap]
rs7142933	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7145905	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7146631	0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7150214	1.00[ASW][hapmap];0.95[LWK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7153565	1.00[ASW][hapmap]
rs7154479	0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7154977	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7157931	1.00[ASW][hapmap];0.82[LWK][hapmap]
rs7158473	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7160824	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs719135	1.00[ASW][hapmap];0.95[LWK][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8011752	0.95[AFR][1000 genomes]
rs8012059	0.83[AFR][1000 genomes]
rs8013329	1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs8014311	1.00[AFR][1000 genomes]
rs8015886	1.00[AFR][1000 genomes]
rs8016268	1.00[ASW][hapmap]
rs8016309	1.00[AFR][1000 genomes]
rs8017263	1.00[ASW][hapmap]
rs8017564	0.83[AFR][1000 genomes]
rs8019167	0.84[LWK][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes]
rs8019983	1.00[ASW][hapmap]
rs8020687	1.00[ASW][hapmap]
rs987859	1.00[ASW][hapmap];0.95[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs9989228	1.00[ASW][hapmap];0.91[LWK][hapmap];0.89[YRI][hapmap];0.90[AFR][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	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv915783	chr14:37607836-38002966	Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1036854	chr14:37609535-38013533	Active TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv542045	chr14:37609535-38013533	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv901639	chr14:37743583-38038468	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv901640	chr14:37782273-37963104	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949227	chr14:37785560-37963104	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv1851939	chr14:37810699-37963104	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv530639	chr14:37837079-37934746	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1043093	chr14:37849742-37928753	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37859400-37878600	Weak transcription	Aorta	Aorta
2	chr14:37867800-37877800	Weak transcription	Fetal Stomach	stomach
3	chr14:37867800-37898800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:37868000-37877600	Weak transcription	Ovary	ovary
5	chr14:37872200-37875400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:37872400-37882800	Weak transcription	Fetal Intestine Small	intestine
7	chr14:37873000-37874600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:37873000-37874600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:37873200-37873600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr14:37873200-37874400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr14:37873400-37874600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links