Variant report

Variant	rs33819
Chromosome Location	chr5:103980038-103980039
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1443071	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs168829	0.84[ASN][1000 genomes]
rs17156785	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2034060	0.83[AMR][1000 genomes]
rs2431106	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2431107	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2431113	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2439978	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2447830	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2447835	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs2447837	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2455315	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs325576	0.86[CHB][hapmap]
rs325577	0.87[CHB][hapmap]
rs33816	0.97[ASN][1000 genomes]
rs33818	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs375770	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs387973	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs394755	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs401327	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs409647	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs411152	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs419682	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs424906	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs454662	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6596580	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6596581	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6596582	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6596583	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7722572	0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882524	chr5:103237745-104019292	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv531969	chr5:103482070-104249804	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv432793	chr5:103693025-104115101	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv428121	chr5:103777677-104094645	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1022638	chr5:103789145-104682389	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv830433	chr5:103862974-103983492	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	esv2752054	chr5:103921670-104289566	Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv882538	chr5:103932079-104019292	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
9	esv2757127	chr5:103939674-103982114	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
10	esv2759363	chr5:103939674-103982114	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
11	nsv1018618	chr5:103955276-104198704	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1022383	chr5:103969150-104086850	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103979200-103981800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr5:103979400-103985400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:103980000-103982600	Enhancers	Colon Smooth Muscle	Colon

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