Variant report

Variant	rs73260317
Chromosome Location	chr14:37539151-37539152
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	chr14:37415215..37416720-chr14:37538798..37540996,2	K562	blood:
2	chr14:37538918..37541164-chr14:37542653..37544836,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11846664	1.00[EUR][1000 genomes]
rs17105856	1.00[EUR][1000 genomes]
rs17105876	1.00[EUR][1000 genomes]
rs17105909	1.00[EUR][1000 genomes]
rs17105921	1.00[EUR][1000 genomes]
rs17105928	1.00[EUR][1000 genomes]
rs17105938	1.00[EUR][1000 genomes]
rs17105941	1.00[EUR][1000 genomes]
rs17105991	1.00[EUR][1000 genomes]
rs17105999	1.00[EUR][1000 genomes]
rs17106020	1.00[EUR][1000 genomes]
rs17106194	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17106252	1.00[EUR][1000 genomes]
rs17106300	1.00[EUR][1000 genomes]
rs17106370	1.00[EUR][1000 genomes]
rs17106427	1.00[EUR][1000 genomes]
rs17106428	1.00[EUR][1000 genomes]
rs17106431	1.00[EUR][1000 genomes]
rs2093087	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2144319	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55764696	1.00[EUR][1000 genomes]
rs55987900	1.00[EUR][1000 genomes]
rs56167909	1.00[EUR][1000 genomes]
rs56395950	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57432181	1.00[EUR][1000 genomes]
rs57545427	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60179583	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60717098	1.00[EUR][1000 genomes]
rs60846053	1.00[EUR][1000 genomes]
rs60910364	1.00[EUR][1000 genomes]
rs61200961	1.00[EUR][1000 genomes]
rs7141866	1.00[EUR][1000 genomes]
rs7147703	1.00[EUR][1000 genomes]
rs73256266	1.00[EUR][1000 genomes]
rs73256270	1.00[EUR][1000 genomes]
rs73256271	1.00[EUR][1000 genomes]
rs73256284	1.00[EUR][1000 genomes]
rs73256290	1.00[EUR][1000 genomes]
rs73256295	1.00[EUR][1000 genomes]
rs73258212	1.00[EUR][1000 genomes]
rs73260392	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73264172	1.00[EUR][1000 genomes]
rs73266178	1.00[EUR][1000 genomes]
rs74045252	1.00[EUR][1000 genomes]
rs74045477	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs8009539	1.00[EUR][1000 genomes]
rs8009729	1.00[EUR][1000 genomes]
rs8012371	0.84[AFR][1000 genomes]
rs9671258	1.00[EUR][1000 genomes]
rs9672077	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1036201	chr14:37498841-37542041	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1037719	chr14:37498841-37546359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1048854	chr14:37505438-37546359	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2327018	chr14:37539150-37539152	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	chr14:37527200-37539800	Weak transcription	Muscle Satellite Cultured Cells	--

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