Variant report

Variant	rs9920024
Chromosome Location	chr15:33015460-33015461
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:33015386-33015727	H1-neurons	neurons:	n/a	n/a
2	BATF	chr15:33015363-33015714	GM12878	blood:	n/a	n/a
3	POLR2A	chr15:33007578-33017851	IMR90	lung:	n/a	n/a
4	FOXA2	chr15:33015425-33015832	A549	lung:	n/a	n/a
5	RUNX3	chr15:33015387-33016105	GM12878	blood:	n/a	n/a
6	PBX3	chr15:33015420-33015687	GM12878	blood:	n/a	chr15:33015588-33015597
7	CHD1	chr15:33007205-33016414	IMR90	lung:	n/a	chr15:33010001-33010011 chr15:33009561-33009571
8	POLR2A	chr15:33009689-33015806	ProgFib	skin:	n/a	n/a
9	POLR2A	chr15:33015301-33015834	H1-neurons	neurons:	n/a	n/a

Variant related genes	Relation type
ENSG00000259721	TF binding region

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1129456	0.92[CEU][hapmap]
rs1258798	1.00[ASN][1000 genomes]
rs13329443	1.00[ASN][1000 genomes]
rs13329491	1.00[ASN][1000 genomes]
rs17228641	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs17525764	0.91[CEU][hapmap]
rs17816363	0.81[CEU][hapmap]
rs17816447	1.00[ASN][1000 genomes]
rs28433691	0.82[EUR][1000 genomes]
rs28436730	0.89[EUR][1000 genomes]
rs28439346	0.82[EUR][1000 genomes]
rs28449413	1.00[ASN][1000 genomes]
rs28473724	0.96[EUR][1000 genomes]
rs28482374	0.91[EUR][1000 genomes]
rs28564029	0.91[EUR][1000 genomes]
rs28574623	1.00[ASN][1000 genomes]
rs28585618	0.83[EUR][1000 genomes]
rs28615915	0.83[EUR][1000 genomes]
rs28617440	0.91[EUR][1000 genomes]
rs28767884	0.89[EUR][1000 genomes]
rs28768389	0.91[EUR][1000 genomes]
rs28840420	0.90[EUR][1000 genomes]
rs3207357	0.96[EUR][1000 genomes]
rs7175986	0.89[EUR][1000 genomes]
rs73384993	1.00[ASN][1000 genomes]
rs73385001	1.00[ASN][1000 genomes]
rs73386805	1.00[ASN][1000 genomes]
rs9920792	0.83[EUR][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	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	nsv456787	chr15:32968923-33023951	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv568916	chr15:32968923-33023951	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33012000-33023200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:33012400-33023200	Weak transcription	HSMM	muscle
3	chr15:33013000-33020400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:33013200-33020800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr15:33013400-33022800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:33013600-33022000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr15:33013600-33023400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr15:33014400-33016400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:33014800-33015600	Genic enhancers	NHDF-Ad	bronchial
10	chr15:33014800-33015800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr15:33014800-33016400	Flanking Active TSS	GM12878-XiMat	blood
12	chr15:33015000-33016400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:33015000-33016600	Strong transcription	NH-A	brain
14	chr15:33015000-33016800	Genic enhancers	Osteobl	bone
15	chr15:33015000-33022000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:33015200-33015600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:33015400-33015600	Enhancers	A549	lung
18	chr15:33015400-33017000	Strong transcription	Muscle Satellite Cultured Cells	--

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