Variant report

Variant	rs10068913
Chromosome Location	chr5:147547906-147547907
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	CEBPB	chr5:147547846-147548123	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
SPINK14	TF binding region

Extended variants
information (count: 70 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10041939	0.80[ASN][1000 genomes]
rs10052031	0.90[ASN][1000 genomes]
rs10055396	0.80[ASN][1000 genomes]
rs10059441	0.80[ASN][1000 genomes]
rs10061827	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10065999	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10068904	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10068916	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10068922	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10068988	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10070470	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10074328	0.90[ASN][1000 genomes]
rs10075227	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10077607	0.80[ASN][1000 genomes]
rs11168034	0.83[AFR][1000 genomes]
rs12653723	0.80[ASN][1000 genomes]
rs12653724	0.80[ASN][1000 genomes]
rs13165271	0.85[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs13169394	0.85[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs13360182	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs1558410	0.90[ASN][1000 genomes]
rs1974627	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1974628	0.90[ASN][1000 genomes]
rs1974629	0.90[ASN][1000 genomes]
rs2159661	0.89[ASN][1000 genomes]
rs2191680	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2191681	0.89[ASN][1000 genomes]
rs2400488	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2400491	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2400492	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2400493	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2400494	0.90[ASN][1000 genomes]
rs2400495	0.90[ASN][1000 genomes]
rs2400496	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2400497	0.90[ASN][1000 genomes]
rs2400498	0.90[ASN][1000 genomes]
rs34339574	0.80[ASN][1000 genomes]
rs35217112	0.80[ASN][1000 genomes]
rs35491588	0.80[ASN][1000 genomes]
rs35696310	0.80[ASN][1000 genomes]
rs36056267	0.80[ASN][1000 genomes]
rs3935572	0.88[AFR][1000 genomes]
rs4254894	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap]
rs4259160	0.90[ASN][1000 genomes]
rs4269285	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4270684	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4419576	0.85[AFR][1000 genomes]
rs4452547	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6580532	0.80[ASN][1000 genomes]
rs6872890	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6881658	0.94[YRI][hapmap]
rs6888999	0.83[AFR][1000 genomes]
rs6894796	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6895745	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs724726	0.83[AFR][1000 genomes]
rs7445725	0.90[ASN][1000 genomes]
rs767568	0.90[ASN][1000 genomes]
rs767569	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs767570	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7703761	0.90[ASN][1000 genomes]
rs7716861	0.80[ASN][1000 genomes]
rs7717500	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7719535	0.80[ASN][1000 genomes]
rs9285669	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9325077	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9325078	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9325084	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv830515	chr5:147460852-147602247	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv968858	chr5:147544134-147548438	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10068913	SPINK6	cis	Esophagus Mucosa	GTEx

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
chromosomal regions: chr1:12345-34567

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