Variant report

Variant	rs12699797
Chromosome Location	chr7:16500335-16500336
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16499530..16502497-chr7:16557938..16560776,2	K562	blood:
2	chr7:16459174..16462298-chr7:16499755..16502845,3	K562	blood:
3	chr7:16499817..16502074-chr7:16502589..16505491,4	K562	blood:

Variant related genes	Relation type
ENSG00000214960	Chromatin interaction
ENSG00000171243	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10085439	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10085489	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10085777	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10499469	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10950622	0.80[EUR][1000 genomes]
rs11761180	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11763476	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11770398	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12532480	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12699795	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12699796	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12699798	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12699799	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12699800	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12699801	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12699802	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17619106	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2141804	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2293672	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2301971	0.86[ASN][1000 genomes]
rs2528472	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2528473	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2704667	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2704668	0.82[EUR][1000 genomes]
rs4719466	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4721504	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56271810	0.86[ASN][1000 genomes]
rs6461257	0.86[ASN][1000 genomes]
rs6950958	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6964287	0.84[ASN][1000 genomes]
rs73074739	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8180829	0.86[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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 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	chr7:16496200-16501000	Weak transcription	Fetal Kidney	kidney
2	chr7:16498600-16500800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:16498800-16500600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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