Variant report

Variant	rs115481420
Chromosome Location	chr4:150066930-150066931
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880247	chr4:150057979-150159936	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1022438	chr4:150066349-150196711	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150066200-150068200	Enhancers	NHDF-Ad	bronchial
2	chr4:150066600-150068400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:150066800-150067200	Enhancers	HSMM	muscle
4	chr4:150066800-150067200	Enhancers	Osteobl	bone
5	chr4:150066800-150067400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:150066800-150067400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:150066800-150067400	Enhancers	NH-A	brain
8	chr4:150066800-150067400	Enhancers	NHLF	lung

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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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