Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10774496	0.93[CHB][hapmap];0.89[JPT][hapmap]
rs10849647	0.93[CHB][hapmap];0.95[JPT][hapmap]
rs10849651	0.93[CHB][hapmap];0.89[JPT][hapmap]
rs10849652	0.93[CHB][hapmap];0.89[JPT][hapmap]
rs10849654	0.87[ASN][1000 genomes]
rs10849656	0.93[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs10849657	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10849658	0.90[ASN][1000 genomes]
rs10849659	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs11064761	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs11064763	0.93[CHB][hapmap];0.95[JPT][hapmap]
rs11064764	0.93[CHB][hapmap];0.95[JPT][hapmap]
rs34765258	0.94[ASN][1000 genomes]
rs4300442	0.93[CHB][hapmap];0.89[JPT][hapmap];0.86[ASN][1000 genomes]
rs4346024	0.90[ASN][1000 genomes]
rs4384428	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs4465416	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs4991185	0.93[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7132771	0.84[EUR][1000 genomes]
rs7301599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7313792	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs7485706	0.81[EUR][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	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv916688	chr12:119801814-120044407	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv899553	chr12:119837250-119876571	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119851600-119872400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:119853000-119853600	Enhancers	Placenta	Placenta
3	chr12:119853000-119853600	Enhancers	Rectal Mucosa Donor 31	rectum

Quick Search: