Variant report

Variant	rs2057274
Chromosome Location	chr14:38021008-38021009
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:38019806..38021457-chr14:38063234..38065481,2	MCF-7	breast:
2	chr14:38014337..38017689-chr14:38019804..38021819,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129514	Chromatin interaction
ENSG00000139865	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10133391	0.88[EUR][1000 genomes]
rs10133438	0.82[ASN][1000 genomes]
rs10144334	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10145473	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10151200	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11156961	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1154688	0.82[ASN][1000 genomes]
rs1158700	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1158701	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1159151	0.82[ASN][1000 genomes]
rs12147939	0.81[AMR][1000 genomes]
rs12884884	0.82[EUR][1000 genomes]
rs1547009	0.82[ASN][1000 genomes]
rs17768343	0.82[EUR][1000 genomes]
rs1884803	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1950824	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1950826	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1956438	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1956439	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1956440	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1980675	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2038438	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28397975	0.82[ASN][1000 genomes]
rs4898640	0.82[ASN][1000 genomes]
rs4900958	0.87[EUR][1000 genomes]
rs4900966	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4900967	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4900969	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4900971	0.82[ASN][1000 genomes]
rs4900972	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7143956	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7146958	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7159456	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7493775	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	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
3	nsv564349	chr14:37890433-38034434	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv901641	chr14:37939401-38040755	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv826923	chr14:38017619-38108645	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38013800-38021200	Weak transcription	Right Ventricle	heart
2	chr14:38013800-38023200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:38014600-38035800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:38016200-38021200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:38016200-38035800	Weak transcription	Stomach Mucosa	stomach
6	chr14:38017000-38021200	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links