Variant report

Variant	rs2238245
Chromosome Location	chr14:72665321-72665322
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs2158986	0.80[AMR][1000 genomes]
rs2158988	0.81[EUR][1000 genomes]
rs2238241	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2238242	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2529647	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4902998	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57141704	0.86[EUR][1000 genomes]
rs6574054	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs699360	0.80[AMR][1000 genomes]
rs699361	0.80[AMR][1000 genomes]
rs699362	0.80[AMR][1000 genomes]
rs8022525	0.81[AMR][1000 genomes]
rs8022968	0.81[AMR][1000 genomes]
rs847270	0.82[AMR][1000 genomes]
rs847271	0.82[AMR][1000 genomes]
rs847272	0.82[AMR][1000 genomes]
rs847274	0.81[AMR][1000 genomes]
rs847275	0.81[AMR][1000 genomes]
rs847276	0.80[AMR][1000 genomes]
rs847277	0.81[AMR][1000 genomes]
rs847278	0.83[AMR][1000 genomes]
rs847279	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs847289	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs847297	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs847302	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs847305	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs847307	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs847310	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs847313	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs847314	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs847318	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs847319	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs847320	0.82[EUR][1000 genomes]
rs847321	0.87[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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	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	chr14:72653600-72683000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:72654400-72670200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:72663000-72666800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr14:72664200-72667200	Weak transcription	Adipose Nuclei	Adipose

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