Variant report

Variant	rs11249899
Chromosome Location	chr8:8845210-8845211
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:8838685..8840996-chr8:8844587..8846741,2	MCF-7	breast:
2	chr8:8844681..8846894-chr8:8850207..8853467,3	K562	blood:
3	chr8:8844911..8847892-chr8:8868363..8870612,2	K562	blood:

Variant related genes	Relation type
ENSG00000104626	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1016512	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1045528	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10503395	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12679527	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13249731	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250919	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13263480	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13273769	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13273871	1.00[ASN][1000 genomes]
rs13274157	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13276537	1.00[ASN][1000 genomes]
rs1430931	0.87[EUR][1000 genomes]
rs28393746	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28405982	1.00[ASN][1000 genomes]
rs28516774	0.89[EUR][1000 genomes]
rs28534948	0.89[EUR][1000 genomes]
rs28812315	0.89[EUR][1000 genomes]
rs2956245	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34111588	0.83[EUR][1000 genomes]
rs34334157	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34391124	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34412730	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34418902	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34712023	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3958881	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841088	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55634245	1.00[ASN][1000 genomes]
rs55696609	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60519586	1.00[ASN][1000 genomes]
rs62492946	0.93[EUR][1000 genomes]
rs66483157	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66869483	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67139167	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67434672	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67575865	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67958495	0.84[EUR][1000 genomes]
rs68043139	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989707	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6993811	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7008080	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7012302	1.00[ASN][1000 genomes]
rs73195799	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197711	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73197712	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7816149	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7816450	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9650628	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	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
3	nsv917117	chr8:8621658-9313799	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv831229	chr8:8751523-8926235	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv610205	chr8:8799111-8891644	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11249899	THEX1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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