Variant report

Variant	rs28663303
Chromosome Location	chr8:8556278-8556279
allele	C/T
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	JUN	chr8:8555865-8556298	K562	blood:	n/a	chr8:8556101-8556112 chr8:8556103-8556110 chr8:8556098-8556109 chr8:8556099-8556108
2	CEBPB	chr8:8556244-8556412	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:8553226..8556449-chr8:8563078..8566145,3	MCF-7	breast:

Variant related genes	Relation type
CLDN23	TF binding region
ENSG00000176305	TF binding region

Extended variants
information (count: 64 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1109618	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11773943	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11777091	0.82[ASN][1000 genomes]
rs11779327	0.82[ASN][1000 genomes]
rs11779524	0.82[ASN][1000 genomes]
rs11780216	0.82[ASN][1000 genomes]
rs11780824	0.86[ASN][1000 genomes]
rs11781841	0.86[ASN][1000 genomes]
rs11783487	0.95[ASN][1000 genomes]
rs11783944	0.91[ASN][1000 genomes]
rs11783950	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11785183	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11786455	0.82[ASN][1000 genomes]
rs11787172	0.95[ASN][1000 genomes]
rs13261926	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1589613	0.82[ASN][1000 genomes]
rs17154599	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17154709	0.82[ASN][1000 genomes]
rs17684466	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28729565	0.84[ASN][1000 genomes]
rs36095989	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4840353	1.00[ASN][1000 genomes]
rs4841012	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4841013	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs55711333	0.83[ASN][1000 genomes]
rs55840094	0.83[ASN][1000 genomes]
rs55874147	0.86[ASN][1000 genomes]
rs56094035	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56102083	0.83[ASN][1000 genomes]
rs56152067	0.86[ASN][1000 genomes]
rs56188408	0.86[ASN][1000 genomes]
rs68168815	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6994131	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7002397	0.83[ASN][1000 genomes]
rs71537846	0.82[AMR][1000 genomes]
rs73192442	0.83[ASN][1000 genomes]
rs73192443	0.83[ASN][1000 genomes]
rs73192444	0.83[ASN][1000 genomes]
rs7816329	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7816427	1.00[ASN][1000 genomes]
rs7819167	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7840561	0.95[ASN][1000 genomes]
rs883647	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs940030	0.84[ASN][1000 genomes]
rs940031	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs940032	1.00[ASN][1000 genomes]
rs9644774	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890331	chr8:8093240-8971100	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1025994	chr8:8108863-8580201	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv1030433	chr8:8130629-8653691	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv539447	chr8:8130629-8653691	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv1033463	chr8:8221922-8674333	Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv539451	chr8:8221922-8674333	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv1019613	chr8:8239352-8636357	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv539452	chr8:8239352-8636357	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv1019606	chr8:8353661-8736992	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	nsv539456	chr8:8353661-8736992	Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
11	nsv995047	chr8:8353662-8857913	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	nsv1016933	chr8:8432279-8624770	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv1022511	chr8:8493992-8737132	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv539457	chr8:8493992-8737132	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv1033340	chr8:8522963-8565946	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
16	nsv539458	chr8:8522963-8565946	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv1028237	chr8:8532992-8588470	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs28663303	C8orf5	Cis_chr	lymphoblastoid	RTeQTL
rs28663303	BLK	Cis_chr	lymphoblastoid	RTeQTL
rs28663303	THEX1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8549800-8558400	Weak transcription	Pancreas	Pancrea
2	chr8:8553800-8556800	Enhancers	Stomach Mucosa	stomach
3	chr8:8554400-8557400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr8:8555600-8557200	Enhancers	Gastric	stomach
5	chr8:8555600-8558400	Weak transcription	Liver	Liver
6	chr8:8555800-8556400	Enhancers	Fetal Intestine Large	intestine
7	chr8:8555800-8556600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:8555800-8556600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:8555800-8558400	Weak transcription	GM12878-XiMat	blood
10	chr8:8556200-8558400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:8556200-8558400	Weak transcription	NHLF	lung
12	chr8:8556200-8558600	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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