Variant report

Variant	rs72922806
Chromosome Location	chr4:130144352-130144353
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56219732	1.00[AMR][1000 genomes]
rs59285303	1.00[AMR][1000 genomes]
rs72924154	1.00[AMR][1000 genomes]
rs72924157	1.00[AMR][1000 genomes]
rs72924167	1.00[AMR][1000 genomes]
rs72926013	1.00[AMR][1000 genomes]
rs72926017	1.00[AMR][1000 genomes]
rs72926020	1.00[AMR][1000 genomes]
rs72926029	1.00[AMR][1000 genomes]
rs72926030	1.00[AMR][1000 genomes]
rs72926072	1.00[AMR][1000 genomes]
rs72926087	1.00[AMR][1000 genomes]
rs72926090	1.00[AMR][1000 genomes]
rs72927922	1.00[AMR][1000 genomes]
rs72927928	1.00[AMR][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	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv879931	chr4:129939775-130178102	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3409155	chr4:130142127-130144675	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3438852	chr4:130142202-130144600	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130144200-130145000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr4:130144200-130145600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:130144200-130146400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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