Variant report

Variant	rs4899430
Chromosome Location	chr14:72759512-72759513
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:72570534..72571227-chr14:72759065..72759718,2	MCF-7	breast:
2	chr14:72570215..72571451-chr14:72758982..72759729,6	MCF-7	breast:
3	chr14:72490629..72491408-chr14:72758856..72759783,5	MCF-7	breast:
4	chr14:72758845..72761499-chr14:72887079..72888301,15	MCF-7	breast:
5	chr14:72398262..72400525-chr14:72758927..72761647,3	MCF-7	breast:
6	chr14:72489255..72491408-chr14:72757396..72759777,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182732	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10146126	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1029616	0.89[YRI][hapmap]
rs10483843	0.90[MEX][hapmap]
rs12184980	0.89[ASW][hapmap];0.90[MEX][hapmap];0.89[YRI][hapmap]
rs1879292	0.89[YRI][hapmap]
rs1996661	0.80[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.81[AMR][1000 genomes]
rs2079500	0.90[MEX][hapmap]
rs2090736	0.81[AMR][1000 genomes]
rs2139596	0.86[TSI][hapmap]
rs2222311	1.00[TSI][hapmap];0.80[YRI][hapmap];0.81[AMR][1000 genomes]
rs2238204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2238205	0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2238206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2238207	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2529476	0.80[AMR][1000 genomes]
rs6574061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6574065	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7144038	0.89[ASW][hapmap];0.89[YRI][hapmap]
rs7151952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.85[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7152907	0.89[ASW][hapmap];0.90[MEX][hapmap];0.89[YRI][hapmap]
rs7156910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs737498	0.90[MEX][hapmap]
rs737499	0.89[ASW][hapmap];0.90[MEX][hapmap];0.89[YRI][hapmap]
rs765221	0.80[MEX][hapmap];0.96[TSI][hapmap]
rs847331	0.93[TSI][hapmap]
rs847334	0.86[TSI][hapmap]
rs847348	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs847349	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs847350	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs847360	0.88[CHB][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap]
rs847362	0.88[CHB][hapmap];0.97[GIH][hapmap];0.89[JPT][hapmap]
rs847364	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4899430	TTC9	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72756800-72759600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr14:72758000-72759600	Enhancers	Fetal Stomach	stomach
3	chr14:72758600-72759600	Enhancers	Ovary	ovary

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