Variant report

Variant	rs10486359
Chromosome Location	chr7:19653111-19653112
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10228147	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10230207	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10242068	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10267686	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10273311	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10282612	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1074858	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10807794	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1158069	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11767221	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12538102	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12700063	0.99[EUR][1000 genomes]
rs13246869	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs13437937	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2058422	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2080017	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2109873	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2109874	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2192476	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2192477	0.81[AMR][1000 genomes]
rs2390142	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2390143	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28407069	0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28460797	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4472416	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4472417	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4509205	0.87[ASN][1000 genomes]
rs4626493	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4719571	0.83[ASN][1000 genomes]
rs4719572	0.83[ASN][1000 genomes]
rs4719573	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4719574	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4719575	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4719576	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4721791	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4721792	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4721794	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6461445	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6461446	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7786622	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7798205	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7802880	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7805790	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7809851	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9655174	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9655175	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887819	chr7:19262091-19658389	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1018601	chr7:19272360-20008881	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
3	esv2752996	chr7:19392086-19684019	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv887824	chr7:19524863-19687779	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1016344	chr7:19574677-19654624	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1032609	chr7:19575555-19654624	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv8068	chr7:19618846-19682421	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19652600-19653400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links