Variant report

Variant	rs59450025
Chromosome Location	chr2:114755094-114755095
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	chr2:114754437..114757265-chr2:114758141..114760380,3	K562	blood:

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

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10173891	1.00[EUR][1000 genomes]
rs10179207	1.00[EUR][1000 genomes]
rs10188927	1.00[EUR][1000 genomes]
rs10195450	1.00[EUR][1000 genomes]
rs10199857	1.00[EUR][1000 genomes]
rs10199930	1.00[EUR][1000 genomes]
rs10204719	1.00[EUR][1000 genomes]
rs10204979	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10208093	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11123215	1.00[EUR][1000 genomes]
rs11895582	1.00[EUR][1000 genomes]
rs11895596	1.00[EUR][1000 genomes]
rs12617393	1.00[EUR][1000 genomes]
rs12621090	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13387748	1.00[EUR][1000 genomes]
rs13393280	1.00[EUR][1000 genomes]
rs13399326	1.00[AMR][1000 genomes]
rs13426411	1.00[EUR][1000 genomes]
rs13428539	1.00[EUR][1000 genomes]
rs13429261	1.00[EUR][1000 genomes]
rs13432142	1.00[EUR][1000 genomes]
rs1467292	1.00[EUR][1000 genomes]
rs1504043	1.00[EUR][1000 genomes]
rs1522915	1.00[EUR][1000 genomes]
rs17040419	1.00[EUR][1000 genomes]
rs2047883	1.00[EUR][1000 genomes]
rs2177263	1.00[EUR][1000 genomes]
rs3828257	1.00[EUR][1000 genomes]
rs4362566	1.00[EUR][1000 genomes]
rs6542179	1.00[EUR][1000 genomes]
rs6706992	1.00[EUR][1000 genomes]
rs6724586	1.00[EUR][1000 genomes]
rs6732402	1.00[EUR][1000 genomes]
rs6735673	1.00[EUR][1000 genomes]
rs6741741	1.00[EUR][1000 genomes]
rs6741785	1.00[EUR][1000 genomes]
rs6742452	1.00[EUR][1000 genomes]
rs6747278	1.00[EUR][1000 genomes]
rs6759040	1.00[EUR][1000 genomes]
rs7561061	1.00[EUR][1000 genomes]
rs7575874	1.00[EUR][1000 genomes]
rs7580099	1.00[EUR][1000 genomes]
rs7581859	1.00[EUR][1000 genomes]
rs924804	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874904	chr2:114751691-115605062	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114736200-114761000	Weak transcription	HSMMtube	muscle
2	chr2:114741200-114761000	Weak transcription	HSMM	muscle
3	chr2:114754000-114755200	Enhancers	HepG2	liver
4	chr2:114754400-114755600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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