Variant report

Variant	rs72726254
Chromosome Location	chr14:65335533-65335534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs17102223	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17102244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951496	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2182034	1.00[AMR][1000 genomes]
rs55796139	1.00[AMR][1000 genomes]
rs56327757	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7147408	1.00[ASN][1000 genomes]
rs72726243	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72726248	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72726253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72726257	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72726258	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72726262	1.00[AMR][1000 genomes]
rs72726263	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72726265	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72726266	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72726269	1.00[AMR][1000 genomes]
rs72726271	1.00[AMR][1000 genomes]
rs72728205	1.00[AMR][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	esv3693408	chr14:65292670-65358576	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
2	nsv516238	chr14:65327288-65358576	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65331600-65335800	Enhancers	Psoas Muscle	Psoas
2	chr14:65331800-65342400	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr14:65332800-65335600	Enhancers	Right Ventricle	heart
4	chr14:65333200-65336000	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr14:65334200-65340800	Weak transcription	Fetal Heart	heart
6	chr14:65334200-65342000	Weak transcription	Right Atrium	heart
7	chr14:65335200-65336000	Enhancers	K562	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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