Variant report

Variant	rs1333727
Chromosome Location	chr1:97681342-97681343
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10783056	0.83[CEU][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs10875056	0.86[EUR][1000 genomes]
rs12046655	0.95[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs12402250	0.86[EUR][1000 genomes]
rs1413239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1931072	0.86[EUR][1000 genomes]
rs2027054	0.83[CEU][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs2039447	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2039448	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3897933	0.83[CEU][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]
rs4511173	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61637399	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs827497	0.90[TSI][hapmap];0.86[EUR][1000 genomes]
rs864335	0.83[EUR][1000 genomes]
rs865242	0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs866129	0.83[CEU][hapmap];0.90[TSI][hapmap];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	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv530048	chr1:97457175-98031501	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1007950	chr1:97466488-98021146	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv533039	chr1:97665736-98343102	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv546861	chr1:97676519-97686036	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
6	nsv546862	chr1:97681342-97685992	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
7	nsv546863	chr1:97681342-97691005	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1333727	CDC14A	cis	parietal	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97658800-97695600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:97659000-97697000	Weak transcription	Liver	Liver
3	chr1:97659800-97696000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr1:97660600-97698600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr1:97663600-97698600	Weak transcription	Primary T cells from cord blood	blood
6	chr1:97666600-97697400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr1:97678200-97698600	Weak transcription	Left Ventricle	heart
8	chr1:97678400-97697400	Weak transcription	Dnd41	blood
9	chr1:97680400-97685200	Weak transcription	Monocytes-CD14+_RO01746	blood

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Input of quick search could be:

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

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