Variant report

Variant	rs4899174
Chromosome Location	chr14:65811400-65811401
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:65810503..65812157-chr14:65814599..65816417,2	K562	blood:
2	chr14:65806797..65809405-chr14:65809997..65812535,2	K562	blood:
3	chr14:65809666..65811577-chr14:65812664..65815660,3	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11158591	0.87[EUR][1000 genomes]
rs11621121	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11621604	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11623920	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11627402	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11627598	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12878872	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12880725	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12881755	0.91[ASN][1000 genomes]
rs12881911	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12882269	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12886005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12886168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12893094	0.80[AMR][1000 genomes]
rs12895337	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1815654	0.88[EUR][1000 genomes]
rs1954052	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902391	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4902393	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7143666	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7152441	0.87[ASN][1000 genomes]
rs7157006	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7158347	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs747541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8014475	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8022094	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832818	chr14:65706859-65882320	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
3	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
4	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65803400-65811600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr14:65803400-65813200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr14:65803400-65813200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr14:65803400-65813400	Weak transcription	NHLF	lung
5	chr14:65803400-65821000	Weak transcription	Esophagus	oesophagus
6	chr14:65807000-65811800	Weak transcription	Gastric	stomach
7	chr14:65807000-65812800	Weak transcription	Fetal Intestine Large	intestine
8	chr14:65807200-65811800	Weak transcription	Stomach Mucosa	stomach
9	chr14:65810400-65812000	Enhancers	Placenta	Placenta

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