Variant report

Variant	rs17106258
Chromosome Location	chr14:37550852-37550853
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11847695	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11848802	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11849630	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11849702	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17106126	1.00[AMR][1000 genomes]
rs17106131	1.00[AMR][1000 genomes]
rs17106144	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17106145	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17106148	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17106239	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17106246	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1950815	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37544400-37552200	Weak transcription	K562	blood
2	chr14:37549800-37552800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:37550200-37552000	Enhancers	Hela-S3	cervix
4	chr14:37550600-37551000	Enhancers	NHEK	skin
5	chr14:37550800-37551200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:37550800-37551800	Weak transcription	HMEC	breast

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

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