Variant report

Variant	rs61057724
Chromosome Location	chr17:17355111-17355112
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs59919193	1.00[AMR][1000 genomes]
rs73288501	1.00[AMR][1000 genomes]
rs73290416	1.00[AMR][1000 genomes]
rs73290417	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73290420	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73290423	1.00[AMR][1000 genomes]
rs73290437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73292314	1.00[AMR][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	nsv482648	chr17:17315268-17455442	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1065710	chr17:17328111-17391443	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv907729	chr17:17338536-17425279	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17349600-17363200	Weak transcription	Right Atrium	heart
2	chr17:17350400-17363400	Weak transcription	Gastric	stomach
3	chr17:17354000-17355600	Enhancers	HepG2	liver
4	chr17:17354200-17358200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr17:17354600-17358000	Weak transcription	Fetal Muscle Leg	muscle
6	chr17:17354800-17355800	Weak transcription	Brain Germinal Matrix	brain
7	chr17:17354800-17368000	Weak transcription	Fetal Thymus	thymus
8	chr17:17355000-17355400	Weak transcription	Spleen	Spleen

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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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