Variant report

Variant	rs72719809
Chromosome Location	chr14:72555724-72555725
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17179470	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72719805	0.93[EUR][1000 genomes]
rs72719810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72719822	0.93[EUR][1000 genomes]
rs72719824	0.93[EUR][1000 genomes]
rs72719825	0.93[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	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

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72551000-72560800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72553400-72556400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr14:72553600-72556000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr14:72553600-72556200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr14:72553600-72556400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:72553600-72556400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:72554600-72555800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr14:72554600-72556800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr14:72555400-72555800	Enhancers	Right Ventricle	heart
10	chr14:72555400-72556800	Enhancers	Right Atrium	heart
11	chr14:72555600-72556800	Enhancers	Left Ventricle	heart
12	chr14:72555600-72560000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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