Variant report

Variant	rs59212716
Chromosome Location	chr7:57029215-57029216
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022563	chr7:56383876-57318888	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1020833	chr7:56511848-57323499	ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
3	nsv538865	chr7:56511848-57323499	ZNF genes & repeats Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
4	nsv1017561	chr7:56512618-57334136	Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
5	nsv1033128	chr7:56787535-57493216	ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
6	nsv1017155	chr7:56795476-57084120	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	esv2761073	chr7:56795488-57116749	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1019894	chr7:56807732-57068728	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1021343	chr7:56807732-57084120	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1016071	chr7:56807732-57116749	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1016541	chr7:56823372-57806010	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1031261	chr7:56949355-57601047	Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
13	nsv970844	chr7:57004618-57052837	ZNF genes & repeats	TF binding region CpG island lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
14	nsv1029803	chr7:57007829-57601047	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
15	esv1811094	chr7:57014904-57095932	ZNF genes & repeats	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
16	nsv888068	chr7:57018980-57116749	ZNF genes & repeats	TF binding region CpG island lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
17	esv1806939	chr7:57028771-57072359	ZNF genes & repeats	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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