Variant report

Variant	rs2695104
Chromosome Location	chr2:178825351-178825352
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:178823421..178826085-chr2:178834912..178837926,3	K562	blood:
2	chr2:178817015..178819167-chr2:178824979..178826962,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10930814	0.81[EUR][1000 genomes]
rs11695211	0.84[ASN][1000 genomes]
rs12463866	0.80[AFR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12469439	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12615720	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1369519	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1369520	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs1405643	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1405644	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1405645	0.87[ASN][1000 genomes]
rs1405646	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1534290	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16865995	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16866042	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1821628	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2037757	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2099476	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2217839	0.87[ASN][1000 genomes]
rs2573080	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2573081	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2573085	0.84[ASN][1000 genomes]
rs2573088	0.90[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2695094	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2695103	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2695111	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2695112	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2695729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2695738	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2695754	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2695760	0.90[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs3108476	0.80[AFR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4893847	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62185280	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6433705	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6745288	0.84[ASN][1000 genomes]
rs6753870	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7573622	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs934807	0.82[EUR][1000 genomes]
rs959157	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv215311	chr2:178822646-178831927	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178823000-178828000	Weak transcription	Ovary	ovary

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