Variant report

Variant	rs9535351
Chromosome Location	chr13:50386753-50386754
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50383200-50387200	Enhancers	Fetal Intestine Small	intestine
2	chr13:50383600-50389400	Enhancers	Fetal Heart	heart
3	chr13:50384200-50390200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr13:50384400-50387400	Enhancers	Fetal Intestine Large	intestine
5	chr13:50384600-50387200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr13:50384800-50389600	Weak transcription	Placenta	Placenta
7	chr13:50385000-50389400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:50385400-50387200	Weak transcription	Fetal Lung	lung
9	chr13:50385600-50386800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr13:50385600-50387200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:50385600-50387800	Weak transcription	A549	lung
12	chr13:50385600-50388200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:50386000-50390400	Enhancers	HepG2	liver
14	chr13:50386200-50388200	Weak transcription	Left Ventricle	heart
15	chr13:50386600-50387200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr13:50386600-50387400	Enhancers	Psoas Muscle	Psoas

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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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