Variant report

Variant	rs73625607
Chromosome Location	chr11:105144898-105144899
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs57893070	1.00[AMR][1000 genomes]
rs58197626	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60121517	1.00[AMR][1000 genomes]
rs60296474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73621583	1.00[AMR][1000 genomes]
rs73621592	1.00[AMR][1000 genomes]
rs73623311	1.00[AMR][1000 genomes]
rs73623315	1.00[AMR][1000 genomes]
rs73623322	1.00[AMR][1000 genomes]
rs73623348	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73623349	0.81[AFR][1000 genomes]
rs73623381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73623395	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73623398	0.80[AFR][1000 genomes]
rs73623399	0.80[AFR][1000 genomes]
rs73623403	1.00[AMR][1000 genomes]
rs73623418	1.00[AMR][1000 genomes]
rs73623422	1.00[AMR][1000 genomes]
rs73623441	1.00[AMR][1000 genomes]
rs73623453	1.00[AMR][1000 genomes]
rs73623454	1.00[AMR][1000 genomes]
rs73623460	1.00[AMR][1000 genomes]
rs73623471	1.00[AMR][1000 genomes]
rs73623473	1.00[AMR][1000 genomes]
rs73623490	1.00[AMR][1000 genomes]
rs73623500	1.00[AMR][1000 genomes]
rs73625107	1.00[AMR][1000 genomes]
rs73625609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7948870	1.00[AMR][1000 genomes]
rs7951819	1.00[AMR][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	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1044970	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv541160	chr11:104809246-105225032	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1049401	chr11:105096619-105225032	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv471	chr11:105116266-105160548	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	1 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	chr11:105144400-105145200	Enhancers	Fetal Heart	heart
2	chr11:105144400-105145600	Enhancers	Brain Hippocampus Middle	brain
3	chr11:105144600-105145600	Enhancers	Brain Substantia Nigra	brain
4	chr11:105144800-105145400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:105144800-105145600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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