Variant report

Variant	rs4866020
Chromosome Location	chr5:50272281-50272282
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:50270770..50272292-chr5:50274416..50276578,2	MCF-7	breast:
2	chr5:50265958..50268570-chr5:50270172..50272797,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARP8-2	chr5:50265757-50272447	NONHSAT101376

Variant related genes	Relation type
ENSG00000251573	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10805506	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10940613	1.00[ASN][1000 genomes]
rs12523135	0.82[ASN][1000 genomes]
rs12657116	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12658921	0.86[ASN][1000 genomes]
rs12659587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162201	0.86[ASN][1000 genomes]
rs13175573	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs13177246	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13182809	0.91[EUR][1000 genomes]
rs1423227	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1545350	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2289879	1.00[ASN][1000 genomes]
rs2289880	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs250216	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs250238	0.83[ASN][1000 genomes]
rs35192063	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35477295	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35894462	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4866019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59135537	0.84[ASN][1000 genomes]
rs622304	0.83[ASN][1000 genomes]
rs66947818	0.87[ASN][1000 genomes]
rs679362	0.83[ASN][1000 genomes]
rs71615992	0.84[ASN][1000 genomes]
rs71615994	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034445	chr5:49986171-50492609	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv598116	chr5:50064292-50318550	Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv830286	chr5:50165805-50374600	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr5:50272200-50272600	Weak transcription	Stomach Smooth Muscle	stomach

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