Variant report

Variant	rs11667107
Chromosome Location	chr19:51498131-51498132
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11084044	0.98[EUR][1000 genomes]
rs11084045	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11084046	0.88[EUR][1000 genomes]
rs11672663	0.85[EUR][1000 genomes]
rs16988799	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16988801	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs4299259	0.98[EUR][1000 genomes]
rs73936105	0.98[EUR][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	nsv1058277	chr19:51488544-51509847	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr19:51496400-51499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr19:51496600-51499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr19:51496600-51502000	Weak transcription	NHEK	skin
4	chr19:51496600-51503000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr19:51498000-51502200	Weak transcription	HMEC	breast
6	chr19:51498000-51503000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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