Variant report

Variant	rs7327323
Chromosome Location	chr13:38521085-38521086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:38520243..38522513-chr13:38539174..38542124,2	K562	blood:
2	chr13:38511957..38514070-chr13:38519300..38521584,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12429858	0.94[ASN][1000 genomes]
rs1337594	0.83[ASN][1000 genomes]
rs1337595	0.81[ASN][1000 genomes]
rs1337605	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1337607	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1415599	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1415628	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1556781	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2210979	0.97[ASN][1000 genomes]
rs2485286	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2485291	0.83[ASN][1000 genomes]
rs2485483	0.87[ASN][1000 genomes]
rs34544559	0.97[ASN][1000 genomes]
rs4943548	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4943551	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6563572	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6563573	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6563574	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71423167	0.83[ASN][1000 genomes]
rs7322764	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7336052	0.96[ASN][1000 genomes]
rs7992543	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7994671	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7994826	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs817729	0.97[ASN][1000 genomes]
rs9315526	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs945858	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs945859	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548093	0.84[ASN][1000 genomes]
rs9548104	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9548107	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9548108	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9548109	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9566279	0.87[ASN][1000 genomes]
rs9576402	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9576405	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9576406	0.83[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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv899996	chr13:38459224-38577056	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv899998	chr13:38480878-38582178	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38519200-38523200	Weak transcription	Fetal Intestine Large	intestine
2	chr13:38519600-38521600	Weak transcription	K562	blood
3	chr13:38520800-38524000	Weak transcription	Fetal Intestine Small	intestine

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