Variant report

Variant	rs551298219
Chromosome Location	chr10:25638369-25638370
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3371273	chr10:25636346-25640744	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2492571	chr10:25637591-25639384	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1997102	chr10:25638093-25639027	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3481618	chr10:25638166-25638932	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3496884	chr10:25638183-25638907	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3496883	chr10:25638187-25638930	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv19471	chr10:25638194-25638834	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3481840	chr10:25638212-25638908	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3481729	chr10:25638220-25638903	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3482063	chr10:25638223-25638862	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3496881	chr10:25638236-25638882	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3481951	chr10:25638272-25638839	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3496882	chr10:25638282-25638842	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv25401	chr10:25638287-25638833	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3482174	chr10:25638287-25638837	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3496885	chr10:25638287-25638837	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25632400-25642600	Weak transcription	Cortex derived primary cultured neurospheres	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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