Variant report

Variant	rs69029
Chromosome Location	chr14:80126358-80126359
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs170251	0.88[CHB][hapmap];0.80[ASN][1000 genomes]
rs170253	0.85[CEU][hapmap]
rs17109638	0.90[CEU][hapmap]
rs172711	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs178350	0.80[ASN][1000 genomes]
rs1816146	0.88[EUR][1000 genomes]
rs182610	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs184347	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs191991	0.87[EUR][1000 genomes]
rs221436	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs221437	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221439	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs221440	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221442	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221443	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221444	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221445	0.90[CEU][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs221446	0.89[CEU][hapmap];0.81[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs221447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221448	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs221449	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs221450	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs221452	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs221455	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs221456	0.90[CHB][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs221459	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs221462	0.81[ASN][1000 genomes]
rs221463	0.80[ASN][1000 genomes]
rs221464	0.80[ASN][1000 genomes]
rs221466	0.94[CHB][hapmap];0.80[ASN][1000 genomes]
rs221471	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221474	0.84[EUR][1000 genomes]
rs221475	0.84[CEU][hapmap]
rs221476	0.95[CEU][hapmap];0.94[CHB][hapmap];0.91[JPT][hapmap]
rs221479	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[JPT][hapmap]
rs221481	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221482	0.90[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221483	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs221484	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs221486	0.84[CEU][hapmap]
rs221487	0.85[CEU][hapmap]
rs221488	0.82[CEU][hapmap]
rs221489	0.83[CEU][hapmap]
rs221492	0.84[CEU][hapmap]
rs221494	0.84[CEU][hapmap]
rs221499	0.89[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs221500	0.85[CEU][hapmap]
rs221501	0.95[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs221502	0.95[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs221503	0.85[CEU][hapmap]
rs221505	0.85[CEU][hapmap]
rs221507	0.95[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs221509	0.85[CEU][hapmap]
rs221510	0.95[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap]
rs221511	0.85[EUR][1000 genomes]
rs221512	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs221513	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs221514	0.95[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2543584	0.84[EUR][1000 genomes]
rs918937	0.94[CEU][hapmap];0.94[CHB][hapmap];0.86[JPT][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9323675	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[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	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:80113200-80135400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:80125200-80126400	Weak transcription	Brain Substantia Nigra	brain
3	chr14:80125600-80127000	Weak transcription	Brain Germinal Matrix	brain
4	chr14:80126200-80126600	Weak transcription	Fetal Kidney	kidney
5	chr14:80126200-80130800	Weak transcription	Brain Cingulate Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links