Variant report

Variant	rs11600983
Chromosome Location	chr11:76970252-76970253
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11607378	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11824060	0.92[ASN][1000 genomes]
rs1793476	0.82[ASN][1000 genomes]
rs1793483	0.82[ASN][1000 genomes]
rs1901821	0.81[EUR][1000 genomes]
rs2007466	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2725812	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2853097	0.83[EUR][1000 genomes]
rs34420077	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4433591	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs473012	0.80[EUR][1000 genomes]
rs478134	0.81[EUR][1000 genomes]
rs482243	0.85[EUR][1000 genomes]
rs487322	0.82[EUR][1000 genomes]
rs489038	0.82[EUR][1000 genomes]
rs492527	0.81[EUR][1000 genomes]
rs4944153	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4944155	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4944158	0.85[EUR][1000 genomes]
rs4945162	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4945166	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4945168	0.82[EUR][1000 genomes]
rs4945169	0.85[EUR][1000 genomes]
rs514191	0.81[EUR][1000 genomes]
rs556696	0.81[EUR][1000 genomes]
rs57129983	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs575662	0.81[EUR][1000 genomes]
rs576079	0.81[EUR][1000 genomes]
rs599437	0.81[EUR][1000 genomes]
rs61901769	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61901771	0.89[EUR][1000 genomes]
rs61901802	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs639857	0.81[EUR][1000 genomes]
rs6592714	0.82[ASN][1000 genomes]
rs6592715	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7118869	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7928731	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534515	chr11:76900813-77035769	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv3424135	chr11:76961603-77277087	Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr11:76957200-76970600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:76965200-76970600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:76965400-76973200	Weak transcription	Liver	Liver

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