Variant report

Variant	rs73683337
Chromosome Location	chr8:63511175-63511176
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10504349	1.00[EUR][1000 genomes]
rs10504350	1.00[EUR][1000 genomes]
rs10504352	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10504353	1.00[EUR][1000 genomes]
rs1079159	1.00[EUR][1000 genomes]
rs1451847	1.00[EUR][1000 genomes]
rs1451852	1.00[EUR][1000 genomes]
rs1480123	1.00[EUR][1000 genomes]
rs1480187	1.00[EUR][1000 genomes]
rs1480188	1.00[EUR][1000 genomes]
rs16928943	1.00[EUR][1000 genomes]
rs16928951	1.00[EUR][1000 genomes]
rs16928969	1.00[EUR][1000 genomes]
rs16929021	1.00[EUR][1000 genomes]
rs16929116	1.00[EUR][1000 genomes]
rs16929139	1.00[EUR][1000 genomes]
rs17840588	1.00[EUR][1000 genomes]
rs2035303	1.00[EUR][1000 genomes]
rs28804670	1.00[EUR][1000 genomes]
rs41362445	1.00[EUR][1000 genomes]
rs55774457	1.00[EUR][1000 genomes]
rs57914735	1.00[EUR][1000 genomes]
rs58977391	1.00[EUR][1000 genomes]
rs59086112	1.00[EUR][1000 genomes]
rs59181770	1.00[EUR][1000 genomes]
rs61299238	1.00[EUR][1000 genomes]
rs6994406	1.00[EUR][1000 genomes]
rs6994555	1.00[EUR][1000 genomes]
rs7001011	1.00[EUR][1000 genomes]
rs7004299	1.00[EUR][1000 genomes]
rs7016380	1.00[EUR][1000 genomes]
rs7016722	1.00[EUR][1000 genomes]
rs7017552	1.00[EUR][1000 genomes]
rs73683323	1.00[EUR][1000 genomes]
rs73683328	1.00[EUR][1000 genomes]
rs73683329	1.00[EUR][1000 genomes]
rs73683336	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73684986	1.00[EUR][1000 genomes]
rs7812896	1.00[EUR][1000 genomes]
rs7816460	1.00[EUR][1000 genomes]
rs7817187	1.00[EUR][1000 genomes]
rs7825429	1.00[EUR][1000 genomes]
rs7837277	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv890959	chr8:63449156-63515522	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 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	chr8:63510600-63512400	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:63511000-63511400	Enhancers	Primary hematopoietic stem cells	blood
3	chr8:63511000-63511800	Enhancers	Fetal Kidney	kidney
4	chr8:63511000-63512000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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