Variant report

Variant	rs28585618
Chromosome Location	chr15:33058001-33058002
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17228641	0.89[EUR][1000 genomes]
rs28436730	0.91[EUR][1000 genomes]
rs28439346	0.96[EUR][1000 genomes]
rs28473724	0.84[EUR][1000 genomes]
rs28482374	0.89[EUR][1000 genomes]
rs28564029	0.89[EUR][1000 genomes]
rs28569405	0.93[EUR][1000 genomes]
rs28574716	0.94[EUR][1000 genomes]
rs28615915	0.97[EUR][1000 genomes]
rs28616589	0.94[EUR][1000 genomes]
rs28617440	0.89[EUR][1000 genomes]
rs28767884	0.91[EUR][1000 genomes]
rs28768389	0.89[EUR][1000 genomes]
rs28840420	0.90[EUR][1000 genomes]
rs3207357	0.84[EUR][1000 genomes]
rs7175986	0.91[EUR][1000 genomes]
rs9920024	0.83[EUR][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	esv2422296	chr15:32798938-33221215	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv456785	chr15:32926076-33352989	Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv568913	chr15:32926076-33352989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv482680	chr15:32958401-33154005	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv832961	chr15:33021177-33134988	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv903977	chr15:33040782-33117302	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	esv2763090	chr15:33042338-33072151	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33049600-33058800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr15:33053000-33059200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr15:33053600-33058200	Weak transcription	NHDF-Ad	bronchial
4	chr15:33053800-33058800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:33054800-33063800	Weak transcription	NHLF	lung
6	chr15:33055000-33058200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:33055800-33065200	Weak transcription	HSMMtube	muscle
8	chr15:33057600-33062400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr15:33057800-33058800	Enhancers	Osteobl	bone
10	chr15:33058000-33063000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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