Variant report

Variant	rs17026536
Chromosome Location	chr4:150833741-150833742
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10004846	1.00[AMR][1000 genomes]
rs10005584	1.00[AMR][1000 genomes]
rs10010230	1.00[AMR][1000 genomes]
rs10017930	1.00[AMR][1000 genomes]
rs10020062	1.00[AMR][1000 genomes]
rs10027651	1.00[AMR][1000 genomes]
rs10027751	1.00[AMR][1000 genomes]
rs10028697	1.00[AMR][1000 genomes]
rs10034848	1.00[AMR][1000 genomes]
rs17026554	1.00[AMR][1000 genomes]
rs28444418	1.00[AMR][1000 genomes]
rs28480105	1.00[AMR][1000 genomes]
rs28485405	1.00[AMR][1000 genomes]
rs28499214	1.00[AMR][1000 genomes]
rs28504685	1.00[AMR][1000 genomes]
rs28515804	1.00[AMR][1000 genomes]
rs28550278	1.00[AMR][1000 genomes]
rs28661715	1.00[AMR][1000 genomes]
rs6839583	1.00[AMR][1000 genomes]
rs7681080	1.00[AMR][1000 genomes]
rs7698116	1.00[AMR][1000 genomes]
rs9992316	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026797	chr4:150246932-151217137	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016169	chr4:150670127-150903827	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537299	chr4:150670127-150903827	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv880254	chr4:150712923-150852782	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv880255	chr4:150777012-150874830	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv932022	chr4:150831733-151419552	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150833000-150834000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:150833600-150835800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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