Variant report

Variant	rs1879288
Chromosome Location	chr14:72740507-72740508
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1002105	0.86[CHB][hapmap];0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs11847225	0.82[CEU][hapmap]
rs11851422	0.82[CEU][hapmap]
rs12147219	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12147220	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12147238	0.84[EUR][1000 genomes]
rs12147792	0.84[EUR][1000 genomes]
rs12147803	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12883470	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12891167	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12897241	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1402065	1.00[CHB][hapmap];0.83[JPT][hapmap];0.86[EUR][1000 genomes]
rs1520327	0.88[EUR][1000 genomes]
rs1520329	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1589301	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17109194	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs17109324	0.84[EUR][1000 genomes]
rs17109573	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17110829	1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs1981604	0.82[EUR][1000 genomes]
rs2079501	0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2238198	0.80[CHB][hapmap]
rs2238200	0.90[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2238203	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2238208	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2238209	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2238210	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2238219	0.82[EUR][1000 genomes]
rs2238220	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2238223	0.84[EUR][1000 genomes]
rs2238224	0.84[EUR][1000 genomes]
rs2238225	0.81[CEU][hapmap]
rs2238226	0.82[CEU][hapmap]
rs2238228	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238229	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238230	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238231	0.84[EUR][1000 genomes]
rs2238232	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238233	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238234	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238235	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238236	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238237	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs2238239	0.90[CEU][hapmap]
rs2238240	0.90[CEU][hapmap]
rs2239252	1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[EUR][1000 genomes]
rs2239253	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes]
rs2239254	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2239256	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap]
rs2239262	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2283393	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs2283394	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2283395	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2283399	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2283400	0.93[EUR][1000 genomes]
rs34122902	0.88[EUR][1000 genomes]
rs34373542	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34755616	0.84[EUR][1000 genomes]
rs34905590	0.84[EUR][1000 genomes]
rs35133217	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35291137	0.86[EUR][1000 genomes]
rs35413081	0.86[EUR][1000 genomes]
rs4324071	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4899429	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4899431	1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes]
rs4899432	1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[EUR][1000 genomes]
rs4903000	0.84[EUR][1000 genomes]
rs4903005	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs4903008	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs4903011	1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[EUR][1000 genomes]
rs55954287	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56263585	0.93[EUR][1000 genomes]
rs66507723	0.84[EUR][1000 genomes]
rs66823874	0.88[EUR][1000 genomes]
rs67838629	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7156265	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7156404	0.82[EUR][1000 genomes]
rs722561	0.82[EUR][1000 genomes]
rs72721816	0.84[EUR][1000 genomes]
rs8006974	0.80[CEU][hapmap]
rs8013850	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8015237	1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs8015476	1.00[CHB][hapmap]
rs8016936	0.82[CEU][hapmap]
rs847251	0.83[JPT][hapmap]
rs847260	0.83[JPT][hapmap]
rs847341	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 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	chr14:72723400-72747600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72732600-72751000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:72740000-72740800	Enhancers	Fetal Heart	heart
4	chr14:72740400-72741000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr14:72740400-72741200	Strong transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links