Variant report

Variant	rs11944750
Chromosome Location	chr4:100455159-100455160
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10007794	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10008896	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10008928	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10013868	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10013883	0.95[ASN][1000 genomes]
rs10020461	0.91[ASN][1000 genomes]
rs10022775	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10026790	0.91[ASN][1000 genomes]
rs10030937	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10516443	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10516444	0.97[ASN][1000 genomes]
rs1054730	0.97[ASN][1000 genomes]
rs1057615	0.91[ASN][1000 genomes]
rs11097668	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11933250	0.91[ASN][1000 genomes]
rs11933337	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11933520	0.91[ASN][1000 genomes]
rs11933937	0.91[ASN][1000 genomes]
rs11934921	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11935423	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11935581	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11937107	0.91[ASN][1000 genomes]
rs11937273	0.91[ASN][1000 genomes]
rs11943031	0.91[ASN][1000 genomes]
rs11944749	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11944752	0.91[ASN][1000 genomes]
rs11946292	0.97[ASN][1000 genomes]
rs11946367	0.80[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs11946658	0.91[ASN][1000 genomes]
rs11947558	0.91[ASN][1000 genomes]
rs1503777	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1503778	0.91[ASN][1000 genomes]
rs17029163	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17531824	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17598226	0.91[ASN][1000 genomes]
rs1800591	0.91[ASN][1000 genomes]
rs1800804	0.91[ASN][1000 genomes]
rs2255119	0.90[ASN][1000 genomes]
rs2637768	0.87[ASN][1000 genomes]
rs2718684	0.87[ASN][1000 genomes]
rs28368786	0.91[ASN][1000 genomes]
rs28376611	0.91[ASN][1000 genomes]
rs28431971	0.85[ASN][1000 genomes]
rs28435607	0.91[ASN][1000 genomes]
rs28444681	0.97[ASN][1000 genomes]
rs28473262	0.91[ASN][1000 genomes]
rs28497720	0.91[ASN][1000 genomes]
rs28500697	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2851225	0.87[ASN][1000 genomes]
rs28595160	0.91[ASN][1000 genomes]
rs28608631	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs28621060	0.94[ASN][1000 genomes]
rs28647519	0.91[ASN][1000 genomes]
rs2866164	0.91[ASN][1000 genomes]
rs28666735	0.90[ASN][1000 genomes]
rs28678377	0.94[ASN][1000 genomes]
rs28704064	0.91[ASN][1000 genomes]
rs28789770	0.91[ASN][1000 genomes]
rs28849180	0.91[ASN][1000 genomes]
rs2903201	0.97[ASN][1000 genomes]
rs3816873	0.91[ASN][1000 genomes]
rs3817083	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4423880	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs45440196	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6815231	0.91[ASN][1000 genomes]
rs6815416	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6825248	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6839296	0.91[ASN][1000 genomes]
rs6841211	0.84[ASN][1000 genomes]
rs6841282	0.88[ASN][1000 genomes]
rs6854911	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72681967	0.97[ASN][1000 genomes]
rs7656665	0.91[ASN][1000 genomes]
rs7661656	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7661964	0.91[ASN][1000 genomes]
rs7682548	0.91[ASN][1000 genomes]
rs7686425	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7687762	0.91[ASN][1000 genomes]
rs7693203	0.91[ASN][1000 genomes]
rs9307240	0.91[ASN][1000 genomes]
rs9997840	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv3584519	chr4:100323870-100477462	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3584522	chr4:100432841-100467011	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3584523	chr4:100437553-100476549	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:100451200-100457000	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:100451200-100457200	Weak transcription	Fetal Intestine Large	intestine

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