Variant report

Variant	rs7690861
Chromosome Location	chr4:81261562-81261563
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81258000-81262000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:81258000-81262800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:81261000-81261800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:81261200-81261600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:81261200-81261600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:81261400-81261800	Strong transcription	Osteobl	bone

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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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