Variant report

Variant	rs567532668
Chromosome Location	chr7:78358200-78358201
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1019355	chr7:78319575-78399845	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv9717	chr7:78357583-78358439	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3476250	chr7:78357727-78358291	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3376177	chr7:78357758-78358271	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3495257	chr7:78357776-78358290	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3495256	chr7:78357777-78358217	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3476249	chr7:78357783-78358257	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3476246	chr7:78357792-78358297	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3476248	chr7:78357794-78358208	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3495258	chr7:78357805-78358229	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3476251	chr7:78357841-78358202	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3495259	chr7:78357841-78358202	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78346800-78361400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr7:78355600-78363400	Weak transcription	Brain Anterior Caudate	brain

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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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