Variant report

Variant	rs16974379
Chromosome Location	chr18:38906377-38906378
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11082228	0.87[EUR][1000 genomes]
rs11875240	0.83[EUR][1000 genomes]
rs11876215	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11877923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12373193	0.86[EUR][1000 genomes]
rs12956831	0.85[EUR][1000 genomes]
rs12956896	0.85[EUR][1000 genomes]
rs12963842	0.87[EUR][1000 genomes]
rs12968299	0.80[EUR][1000 genomes]
rs1496819	0.86[EUR][1000 genomes]
rs16974401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1845925	0.87[EUR][1000 genomes]
rs2703163	0.85[EUR][1000 genomes]
rs2848784	0.85[EUR][1000 genomes]
rs34298584	0.83[EUR][1000 genomes]
rs34736827	0.87[EUR][1000 genomes]
rs58843487	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59169117	0.84[AFR][1000 genomes]
rs6507417	0.86[EUR][1000 genomes]
rs7239092	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9675507	0.87[EUR][1000 genomes]
rs9955082	0.85[AFR][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	nsv909564	chr18:38739067-39179256	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv833629	chr18:38791940-38959145	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv833630	chr18:38817119-39012222	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1792942	chr18:38843538-38941569	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases
7	esv1827680	chr18:38843538-38941569	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases
8	esv1836442	chr18:38843538-38941569	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:38902800-38906400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:38902800-38906400	Enhancers	Hela-S3	cervix
3	chr18:38902800-38906600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr18:38902800-38906600	Enhancers	NHEK	skin
5	chr18:38902800-38907000	Enhancers	HMEC	breast
6	chr18:38906200-38906400	Enhancers	NH-A	brain
7	chr18:38906200-38906600	Enhancers	Muscle Satellite Cultured Cells	--

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