Variant report

Variant	rs73750229
Chromosome Location	chr5:41043469-41043470
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	chr5:41037388..41039310-chr5:41042420..41044059,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1035498	1.00[AMR][1000 genomes]
rs16870881	1.00[AMR][1000 genomes]
rs16870939	1.00[AMR][1000 genomes]
rs16870948	1.00[AMR][1000 genomes]
rs55721014	1.00[AMR][1000 genomes]
rs55752804	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56364240	1.00[AMR][1000 genomes]
rs57323128	1.00[AMR][1000 genomes]
rs57772524	1.00[AMR][1000 genomes]
rs57893040	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57907280	1.00[AMR][1000 genomes]
rs59070453	1.00[AMR][1000 genomes]
rs59800950	1.00[AMR][1000 genomes]
rs59803945	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60746065	1.00[AMR][1000 genomes]
rs60996401	1.00[AMR][1000 genomes]
rs61050629	1.00[AMR][1000 genomes]
rs61111492	1.00[AMR][1000 genomes]
rs61622113	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6451561	1.00[AMR][1000 genomes]
rs6451563	1.00[AMR][1000 genomes]
rs6872142	1.00[AMR][1000 genomes]
rs6880534	1.00[AMR][1000 genomes]
rs6886587	1.00[AMR][1000 genomes]
rs6896011	1.00[AMR][1000 genomes]
rs6896183	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73750256	1.00[AMR][1000 genomes]
rs73750291	1.00[AMR][1000 genomes]
rs73750292	1.00[AMR][1000 genomes]
rs73750295	1.00[AMR][1000 genomes]
rs73750296	1.00[AMR][1000 genomes]
rs73750297	1.00[AMR][1000 genomes]
rs73750298	1.00[AMR][1000 genomes]
rs73750299	1.00[AMR][1000 genomes]
rs73750300	1.00[AMR][1000 genomes]
rs73750301	1.00[AMR][1000 genomes]
rs73750302	1.00[AMR][1000 genomes]
rs73753104	1.00[AMR][1000 genomes]
rs73753105	1.00[AMR][1000 genomes]
rs73753106	1.00[AMR][1000 genomes]
rs73753109	1.00[AMR][1000 genomes]
rs73753111	1.00[AMR][1000 genomes]
rs73753113	1.00[AMR][1000 genomes]
rs73753115	1.00[AMR][1000 genomes]
rs7718212	1.00[AMR][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	nsv830268	chr5:40897361-41138366	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr5:41043000-41044000	Enhancers	Fetal Intestine Large	intestine
2	chr5:41043200-41043800	Enhancers	Fetal Intestine Small	intestine
3	chr5:41043400-41043600	Enhancers	Liver	Liver

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