Variant report

Variant	rs17069919
Chromosome Location	chr6:140638462-140638463
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17069827	0.84[YRI][hapmap]
rs17069896	0.97[EUR][1000 genomes]
rs17069929	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17069951	0.87[EUR][1000 genomes]
rs34350432	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55989526	0.87[EUR][1000 genomes]
rs60519960	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6570391	0.95[LWK][hapmap]
rs6570397	0.84[EUR][1000 genomes]
rs6901224	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6915302	0.87[EUR][1000 genomes]
rs6938047	0.87[EUR][1000 genomes]
rs7743754	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1016532	chr6:140174639-141029988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv1015293	chr6:140544956-140798437	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv817390	chr6:140558103-141166039	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 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	chr6:140632800-140639800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:140634600-140638800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr6:140636800-140639000	Weak transcription	Liver	Liver
4	chr6:140637600-140641600	Enhancers	Fetal Intestine Small	intestine
5	chr6:140637800-140639000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr6:140637800-140640000	Weak transcription	Placenta	Placenta
7	chr6:140637800-140640200	Enhancers	Fetal Intestine Large	intestine
8	chr6:140638400-140639400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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