Variant report

Variant	rs67292864
Chromosome Location	chr2:127203923-127203924
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11674115	0.80[EUR][1000 genomes]
rs11674405	0.80[EUR][1000 genomes]
rs11675808	0.82[EUR][1000 genomes]
rs11684984	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11687739	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11688466	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11694971	0.80[EUR][1000 genomes]
rs12993851	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12996594	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12996629	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12999041	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13001087	0.80[EUR][1000 genomes]
rs13001322	0.80[EUR][1000 genomes]
rs13002409	0.84[EUR][1000 genomes]
rs13002851	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13003278	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13008004	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13010045	0.80[AMR][1000 genomes]
rs13020607	0.80[AMR][1000 genomes]
rs13020846	0.80[EUR][1000 genomes]
rs13023737	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13033014	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13034238	0.80[AMR][1000 genomes]
rs1387284	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs243417	0.80[AMR][1000 genomes]
rs34087027	0.80[AMR][1000 genomes]
rs34228135	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34653086	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34690725	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34731630	0.80[AMR][1000 genomes]
rs34939949	0.80[AMR][1000 genomes]
rs34961369	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34981967	0.80[AMR][1000 genomes]
rs35012492	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35338260	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35371374	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35506144	0.80[AMR][1000 genomes]
rs35683961	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35703634	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs359688	0.80[AMR][1000 genomes]
rs359704	0.80[AMR][1000 genomes]
rs359708	0.80[AMR][1000 genomes]
rs36061035	0.80[AMR][1000 genomes]
rs36109238	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55733801	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56100722	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56332215	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66530889	0.80[AMR][1000 genomes]
rs66701958	0.80[AMR][1000 genomes]
rs66815786	0.80[AMR][1000 genomes]
rs66993274	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67155347	0.80[AMR][1000 genomes]
rs67271291	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67323263	0.81[AMR][1000 genomes]
rs67960481	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72831488	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72831489	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72843721	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013181	chr2:126451639-127246965	Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv997962	chr2:126464195-127234384	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1001995	chr2:126506739-127314488	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv534297	chr2:126506966-127245682	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1002265	chr2:127029745-127733458	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv535919	chr2:127029745-127733458	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv874999	chr2:127068140-127218915	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv834364	chr2:127100752-127267070	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 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	chr2:127203400-127204000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:127203400-127204000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:127203800-127204200	Enhancers	Adipose Nuclei	Adipose
4	chr2:127203800-127204200	Enhancers	Left Ventricle	heart
5	chr2:127203800-127204400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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