Variant report

Variant	rs7955364
Chromosome Location	chr12:47126855-47126856
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10161209	0.85[CHB][hapmap];0.86[CHD][hapmap]
rs11183610	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12301214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12307687	1.00[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12581848	0.85[CHB][hapmap]
rs17097091	0.85[CHB][hapmap]
rs17097141	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs17097246	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17097332	0.85[CHB][hapmap]
rs180431	1.00[MEX][hapmap]
rs2287470	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs235621	0.82[MEX][hapmap]
rs2897979	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs3862137	0.84[CHB][hapmap]
rs4768740	0.90[MEX][hapmap]
rs4768746	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs4768747	0.96[AMR][1000 genomes]
rs4768749	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4768758	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4768759	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs57349356	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6582676	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7133051	0.81[AMR][1000 genomes]
rs7310614	0.90[MEX][hapmap];0.81[AMR][1000 genomes]
rs7311414	0.81[AMR][1000 genomes]
rs7315740	0.81[AMR][1000 genomes]
rs73282105	0.81[AMR][1000 genomes]
rs73282110	0.81[AMR][1000 genomes]
rs7971812	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7979449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs977069	0.82[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv3416674	chr12:46988689-47178369	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv558783	chr12:46996632-47144856	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr12:47121800-47131800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:47122800-47127800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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