Variant report

Variant	rs7917742
Chromosome Location	chr10:50538473-50538474
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	chr10:50536963..50540512-chr10:50542123..50548139,6	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10745258	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10776549	1.00[EUR][1000 genomes]
rs10776552	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10776556	0.92[AMR][1000 genomes]
rs10776559	1.00[EUR][1000 genomes]
rs10776564	1.00[EUR][1000 genomes]
rs10857457	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10857459	1.00[EUR][1000 genomes]
rs2377945	1.00[EUR][1000 genomes]
rs2377947	1.00[EUR][1000 genomes]
rs2377967	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2377973	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2377974	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2889795	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2889796	1.00[EUR][1000 genomes]
rs4012230	1.00[EUR][1000 genomes]
rs4012231	1.00[EUR][1000 genomes]
rs4240502	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4641382	1.00[EUR][1000 genomes]
rs4838374	1.00[EUR][1000 genomes]
rs4838380	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4838382	1.00[EUR][1000 genomes]
rs4838385	0.88[YRI][hapmap]
rs4838471	1.00[EUR][1000 genomes]
rs4838477	1.00[EUR][1000 genomes]
rs4838478	1.00[EUR][1000 genomes]
rs4838488	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4838499	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4838508	1.00[EUR][1000 genomes]
rs4838509	1.00[EUR][1000 genomes]
rs6537511	1.00[EUR][1000 genomes]
rs6537531	1.00[EUR][1000 genomes]
rs7068929	1.00[EUR][1000 genomes]
rs7076165	1.00[EUR][1000 genomes]
rs7078936	0.83[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7080495	1.00[EUR][1000 genomes]
rs7082469	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7084819	1.00[EUR][1000 genomes]
rs7085282	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7088113	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7094465	1.00[EUR][1000 genomes]
rs7094900	1.00[EUR][1000 genomes]
rs7095890	1.00[EUR][1000 genomes]
rs7099166	1.00[EUR][1000 genomes]
rs74130904	1.00[EUR][1000 genomes]
rs74133121	1.00[EUR][1000 genomes]
rs74133124	1.00[EUR][1000 genomes]
rs7893653	1.00[EUR][1000 genomes]
rs7896694	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7902727	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7910727	1.00[EUR][1000 genomes]
rs7923632	1.00[EUR][1000 genomes]
rs9663345	1.00[EUR][1000 genomes]
rs9665575	1.00[EUR][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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv895376	chr10:50480164-50557211	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50531800-50547800	Weak transcription	Pancreas	Pancrea
2	chr10:50533000-50540000	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:50534800-50541000	Weak transcription	Right Ventricle	heart
4	chr10:50535800-50541000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:50537600-50542800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr10:50537600-50542800	Weak transcription	Skeletal Muscle Male	skeletal muscle

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