Variant report

Variant	rs55757800
Chromosome Location	chr15:58290731-58290732
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:58283520..58285614-chr15:58290103..58292837,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10518951	0.90[EUR][1000 genomes]
rs1078777	0.89[EUR][1000 genomes]
rs12591551	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12591715	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12591835	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12592773	0.89[EUR][1000 genomes]
rs12592810	0.89[EUR][1000 genomes]
rs12593050	0.90[EUR][1000 genomes]
rs12593414	0.89[EUR][1000 genomes]
rs12594689	0.88[EUR][1000 genomes]
rs12595264	0.88[EUR][1000 genomes]
rs1372367	0.89[EUR][1000 genomes]
rs16939707	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16939727	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16939733	0.81[EUR][1000 genomes]
rs16953355	0.85[EUR][1000 genomes]
rs16977858	0.90[EUR][1000 genomes]
rs16977861	0.90[EUR][1000 genomes]
rs16977865	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16977883	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1837850	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1874157	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1874158	0.83[EUR][1000 genomes]
rs34134903	1.00[AFR][1000 genomes]
rs34165083	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34570545	1.00[AFR][1000 genomes]
rs35016264	0.87[EUR][1000 genomes]
rs35056852	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35385267	0.89[EUR][1000 genomes]
rs35912910	0.90[EUR][1000 genomes]
rs3825778	0.82[EUR][1000 genomes]
rs4646561	0.88[EUR][1000 genomes]
rs4646565	0.87[EUR][1000 genomes]
rs4646574	0.89[EUR][1000 genomes]
rs4646578	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4646583	0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4646587	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4646591	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4646601	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4646608	0.92[EUR][1000 genomes]
rs4646618	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs4646632	0.89[EUR][1000 genomes]
rs4646637	0.87[EUR][1000 genomes]
rs55723752	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs55866609	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56066922	0.89[EUR][1000 genomes]
rs56141372	0.90[EUR][1000 genomes]
rs56183601	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56280454	0.90[EUR][1000 genomes]
rs56404147	0.90[EUR][1000 genomes]
rs7161823	0.89[EUR][1000 genomes]
rs7178015	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs74017072	0.90[EUR][1000 genomes]
rs74017096	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7495284	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8041300	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038667	chr15:57933076-58481870	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv542400	chr15:57933076-58481870	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv833023	chr15:58161839-58340174	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv569593	chr15:58201698-58308650	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv904261	chr15:58258424-58347260	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58285400-58301400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:58288800-58291600	Weak transcription	Fetal Kidney	kidney
3	chr15:58289000-58292400	Weak transcription	K562	blood
4	chr15:58289800-58299000	Weak transcription	Fetal Lung	lung

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