Variant report

Variant	rs7776758
Chromosome Location	chr7:16326073-16326074
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:16325178..16329293-chr7:16335508..16338297,3	K562	blood:
2	chr7:16317326..16322342-chr7:16324212..16328939,6	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10231565	0.81[EUR][1000 genomes]
rs10261188	0.82[ASN][1000 genomes]
rs10275672	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10277201	0.82[EUR][1000 genomes]
rs10277820	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10282434	0.82[ASN][1000 genomes]
rs10486789	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12155478	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12537719	0.91[ASN][1000 genomes]
rs12667765	0.81[ASN][1000 genomes]
rs12673171	0.81[EUR][1000 genomes]
rs12699779	0.80[ASN][1000 genomes]
rs12699780	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12699781	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12699782	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12699783	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12699784	0.81[EUR][1000 genomes]
rs13226547	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13233751	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13237371	0.80[EUR][1000 genomes]
rs17169411	0.90[EUR][1000 genomes]
rs1859421	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1990019	0.90[EUR][1000 genomes]
rs2107590	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2158487	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2189732	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2189736	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2214625	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2389594	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2892804	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4236287	0.81[EUR][1000 genomes]
rs4349896	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4529354	0.81[ASN][1000 genomes]
rs4565368	0.81[EUR][1000 genomes]
rs4602788	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4721486	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4721488	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61666208	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62441880	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62441884	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6461234	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6948602	0.90[EUR][1000 genomes]
rs6956615	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6968139	0.80[EUR][1000 genomes]
rs6975353	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6977050	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6979436	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6980295	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7459327	0.80[EUR][1000 genomes];0.91[ASN][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	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	nsv948950	chr7:16168925-16395434	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2757214	chr7:16236162-16334228	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	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
5	nsv1022388	chr7:16251992-16431864	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1022814	chr7:16262300-16339988	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16312400-16332800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:16313600-16348200	Weak transcription	Gastric	stomach
3	chr7:16320600-16329200	ZNF genes & repeats	K562	blood

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