Variant report

Variant	rs16939716
Chromosome Location	chr15:58335835-58335836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1441817	1.00[MEX][hapmap]
rs16939647	1.00[EUR][1000 genomes]
rs16939660	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16939661	1.00[EUR][1000 genomes]
rs16939714	1.00[EUR][1000 genomes]
rs16977872	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16977873	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2063902	1.00[CEU][hapmap]
rs2642656	1.00[CEU][hapmap]
rs34682734	1.00[EUR][1000 genomes]
rs34834301	1.00[EUR][1000 genomes]
rs35153668	1.00[EUR][1000 genomes]
rs35636428	1.00[EUR][1000 genomes]
rs4646634	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs74017101	1.00[EUR][1000 genomes]
rs74018811	1.00[EUR][1000 genomes]
rs74018812	1.00[EUR][1000 genomes]
rs74018813	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	nsv1038667	chr15:57933076-58481870	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv542400	chr15:57933076-58481870	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv833023	chr15:58161839-58340174	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv904261	chr15:58258424-58347260	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58331600-58336000	Genic enhancers	K562	blood
2	chr15:58332200-58338200	Weak transcription	Fetal Intestine Large	intestine
3	chr15:58333400-58336400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr15:58333800-58338200	Weak transcription	Fetal Intestine Small	intestine
5	chr15:58334800-58336400	Enhancers	Fetal Lung	lung
6	chr15:58335000-58336800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:58335200-58336200	Enhancers	Small Intestine	intestine
8	chr15:58335600-58336200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr15:58335600-58336200	Enhancers	HMEC	breast
10	chr15:58335600-58336400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr15:58335800-58336000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:58335800-58336200	Enhancers	Primary hematopoietic stem cells	blood
13	chr15:58335800-58336200	Enhancers	Fetal Stomach	stomach
14	chr15:58335800-58338200	Weak transcription	Fetal Kidney	kidney

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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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