Variant report

Variant	rs13134790
Chromosome Location	chr4:76211824-76211825
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:76210768..76213178-chr4:76214495..76216137,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11099473	0.81[ASN][1000 genomes]
rs11730506	0.81[ASN][1000 genomes]
rs11730512	0.81[ASN][1000 genomes]
rs13116975	0.81[ASN][1000 genomes]
rs13133669	0.81[ASN][1000 genomes]
rs13143121	0.81[ASN][1000 genomes]
rs1580768	0.81[ASN][1000 genomes]
rs1580769	0.81[ASN][1000 genomes]
rs1603544	0.85[ASN][1000 genomes]
rs1603545	0.81[ASN][1000 genomes]
rs2087968	0.81[ASN][1000 genomes]
rs2867289	0.85[ASN][1000 genomes]
rs2867290	0.81[ASN][1000 genomes]
rs34605885	0.85[ASN][1000 genomes]
rs34784867	0.85[ASN][1000 genomes]
rs35380097	0.85[ASN][1000 genomes]
rs4859533	0.85[ASN][1000 genomes]
rs4859951	0.81[ASN][1000 genomes]
rs4859954	0.85[ASN][1000 genomes]
rs6812231	0.81[ASN][1000 genomes]
rs6812639	0.81[ASN][1000 genomes]
rs6819230	0.84[ASN][1000 genomes]
rs6832205	0.81[ASN][1000 genomes]
rs6851089	0.81[ASN][1000 genomes]
rs7659569	0.81[ASN][1000 genomes]
rs7662192	0.85[ASN][1000 genomes]
rs7664815	0.81[ASN][1000 genomes]
rs7664835	0.81[ASN][1000 genomes]
rs7665085	0.81[ASN][1000 genomes]
rs7678341	0.81[ASN][1000 genomes]
rs7696346	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005324	chr4:75689880-76233555	Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv537142	chr4:75689880-76233555	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1010552	chr4:76064415-76325430	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv594686	chr4:76139891-76212995	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv998511	chr4:76184807-76398377	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	esv2763368	chr4:76190070-76387413	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76211200-76213400	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr4:76211800-76213600	Enhancers	Fetal Intestine Large	intestine
3	chr4:76211800-76213600	Enhancers	Fetal Intestine Small	intestine

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