Variant report

Variant	rs7486973
Chromosome Location	chr12:86084166-86084167
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10506924	0.88[EUR][1000 genomes]
rs10779190	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10779191	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10779192	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10862997	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs10863034	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs10863035	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs10863045	0.81[ASN][1000 genomes]
rs10863046	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10863047	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10863049	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10863050	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10863052	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10863054	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10863057	0.88[EUR][1000 genomes]
rs10863061	0.80[ASN][1000 genomes]
rs11116964	0.82[ASN][1000 genomes]
rs11116971	0.84[ASN][1000 genomes]
rs11116991	0.86[ASN][1000 genomes]
rs11116996	0.86[ASN][1000 genomes]
rs11117003	0.80[ASN][1000 genomes]
rs12230239	0.86[ASN][1000 genomes]
rs12308693	0.80[ASN][1000 genomes]
rs12308694	0.80[ASN][1000 genomes]
rs12811153	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17013257	0.87[ASN][1000 genomes]
rs2199506	0.80[ASN][1000 genomes]
rs2219718	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2405260	0.80[ASN][1000 genomes]
rs2897094	0.88[EUR][1000 genomes]
rs34929726	0.84[EUR][1000 genomes]
rs4897821	0.87[ASN][1000 genomes]
rs4897822	0.88[EUR][1000 genomes]
rs4897837	0.88[EUR][1000 genomes]
rs4897838	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4897841	0.99[ASN][1000 genomes]
rs7302561	0.87[EUR][1000 genomes]
rs7959638	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs922341	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054573	chr12:85658602-86235433	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1035600	chr12:85661373-86235433	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2751125	chr12:85884858-86098240	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1043253	chr12:85888151-86125364	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1054475	chr12:85985510-86175711	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv541561	chr12:85985510-86175711	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86083000-86084200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr12:86083400-86084600	Weak transcription	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links