Variant report

Variant	rs4902753
Chromosome Location	chr14:70216364-70216365
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:70210188..70218336-chr14:70231974..70235461,17	MCF-7	breast:
2	chr14:70213284..70215465-chr14:70216209..70218771,2	MCF-7	breast:
3	chr14:70106414..70108074-chr14:70216231..70218583,2	K562	blood:
4	chr14:70215666..70217625-chr14:70221053..70222945,2	K562	blood:

Variant related genes	Relation type
ENSG00000100650	Chromatin interaction

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10130926	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10136397	0.88[EUR][1000 genomes]
rs10142027	0.87[ASN][1000 genomes]
rs10142031	0.87[ASN][1000 genomes]
rs10142686	0.88[ASN][1000 genomes]
rs10143223	0.90[ASN][1000 genomes]
rs10146537	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10148404	0.88[EUR][1000 genomes]
rs10151895	0.93[ASN][1000 genomes]
rs10459536	0.94[ASN][1000 genomes]
rs11620808	0.88[EUR][1000 genomes]
rs11621916	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11622580	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11622925	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11623262	0.90[EUR][1000 genomes]
rs11624523	0.94[ASN][1000 genomes]
rs11624532	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11625731	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11625932	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11627012	0.90[EUR][1000 genomes]
rs11627089	0.88[EUR][1000 genomes]
rs11628423	0.90[EUR][1000 genomes]
rs11628546	0.90[EUR][1000 genomes]
rs11628665	0.88[EUR][1000 genomes]
rs12431573	0.81[ASN][1000 genomes]
rs13313365	0.88[EUR][1000 genomes]
rs13313366	0.88[EUR][1000 genomes]
rs14411	0.88[EUR][1000 genomes]
rs17328	0.81[ASN][1000 genomes]
rs1953399	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1953400	0.95[ASN][1000 genomes]
rs2148503	0.94[ASN][1000 genomes]
rs2148505	0.91[ASN][1000 genomes]
rs2332167	0.94[ASN][1000 genomes]
rs28404963	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28437671	0.88[EUR][1000 genomes]
rs28437822	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28480224	0.83[EUR][1000 genomes]
rs2877595	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28785205	0.90[EUR][1000 genomes]
rs28847646	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3104	0.92[ASN][1000 genomes]
rs3784152	0.91[ASN][1000 genomes]
rs3784153	0.91[ASN][1000 genomes]
rs3809399	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4646285	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4646286	0.84[ASN][1000 genomes]
rs4646297	0.91[ASN][1000 genomes]
rs4899311	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4899313	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4902752	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902755	0.94[ASN][1000 genomes]
rs55724465	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55987626	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56074637	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56140822	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56177148	0.88[EUR][1000 genomes]
rs57492222	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58582364	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59066042	0.88[EUR][1000 genomes]
rs59172911	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60442313	0.94[ASN][1000 genomes]
rs61356864	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6573905	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573906	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573907	0.95[ASN][1000 genomes]
rs6573908	0.89[ASN][1000 genomes]
rs7142868	0.95[ASN][1000 genomes]
rs7153496	0.94[ASN][1000 genomes]
rs7153985	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7154439	0.84[ASN][1000 genomes]
rs7160953	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7161476	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72725718	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72725724	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72725740	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72725743	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72725745	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72725776	0.81[EUR][1000 genomes]
rs72725780	0.81[EUR][1000 genomes]
rs8010836	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8011311	0.90[ASN][1000 genomes]
rs8013598	0.90[ASN][1000 genomes]
rs8014236	0.90[ASN][1000 genomes]
rs8021735	0.81[ASN][1000 genomes]
rs9944036	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 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	chr14:70212800-70216600	Enhancers	HepG2	liver
2	chr14:70213200-70218000	Enhancers	Fetal Intestine Small	intestine
3	chr14:70213800-70216600	Weak transcription	K562	blood
4	chr14:70215000-70218000	Enhancers	Fetal Intestine Large	intestine
5	chr14:70216000-70217600	Enhancers	Liver	Liver
6	chr14:70216000-70218000	Enhancers	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links