Variant report

Variant	rs11241424
Chromosome Location	chr5:116739804-116739805
allele	A/T
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:27)

rs_ID	r²[population]
rs10065401	0.83[YRI][hapmap]
rs10075994	0.83[CHB][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1030462	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13164082	0.91[EUR][1000 genomes]
rs13183369	0.93[ASN][1000 genomes]
rs13358449	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13358452	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1428048	0.91[JPT][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2007303	0.84[ASN][1000 genomes]
rs2560593	0.84[ASN][1000 genomes]
rs2560595	0.87[ASN][1000 genomes]
rs2560598	0.81[ASN][1000 genomes]
rs2624459	0.84[ASN][1000 genomes]
rs2624462	0.84[ASN][1000 genomes]
rs2624482	0.81[ASN][1000 genomes]
rs2900102	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4455596	0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4481381	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4587112	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4920870	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4920871	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4920965	0.84[EUR][1000 genomes]
rs6875942	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7714703	0.83[JPT][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7732741	0.87[CHB][hapmap];0.91[JPT][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs950073	0.84[ASN][1000 genomes]
rs950074	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[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	nsv882755	chr5:116647725-116748877	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv830457	chr5:116724777-116875060	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv599487	chr5:116732456-116772093	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116739200-116740000	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr5:116739800-116740400	Active TSS	Placenta	Placenta

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