Variant report

Variant	rs36080287
Chromosome Location	chr14:85616188-85616189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10147553	0.87[ASN][1000 genomes]
rs10498579	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12100468	0.85[ASN][1000 genomes]
rs12432779	0.83[ASN][1000 genomes]
rs12435632	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12879255	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12892485	0.99[ASN][1000 genomes]
rs12895341	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12897852	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1375568	0.82[ASN][1000 genomes]
rs1375569	0.82[ASN][1000 genomes]
rs1449411	0.84[ASN][1000 genomes]
rs1449413	0.83[ASN][1000 genomes]
rs1449430	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1449431	0.84[ASN][1000 genomes]
rs1667543	0.83[ASN][1000 genomes]
rs17120779	0.93[ASN][1000 genomes]
rs1767423	0.82[ASN][1000 genomes]
rs17796484	0.93[ASN][1000 genomes]
rs2372836	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2372841	0.94[ASN][1000 genomes]
rs2372846	0.88[ASN][1000 genomes]
rs2888425	0.84[ASN][1000 genomes]
rs2888426	0.93[ASN][1000 genomes]
rs4243673	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4577003	0.89[ASN][1000 genomes]
rs4904236	0.85[ASN][1000 genomes]
rs4904237	1.00[AFR][1000 genomes]
rs67029848	1.00[AFR][1000 genomes]
rs7143105	0.88[ASN][1000 genomes]
rs7151475	0.85[ASN][1000 genomes]
rs7152160	0.85[ASN][1000 genomes]
rs72685722	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1048026	chr14:85330544-85686322	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3401331	chr14:85332747-85716351	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv565423	chr14:85427846-85638746	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv832846	chr14:85517736-85715650	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv456355	chr14:85565987-85616803	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv565425	chr14:85565987-85616803	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85614600-85617400	Enhancers	Fetal Intestine Large	intestine

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