Variant report

Variant	rs73486524
Chromosome Location	chr11:34057923-34057924
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34055000-34059600	Enhancers	Placenta	Placenta
2	chr11:34055600-34059600	Enhancers	K562	blood
3	chr11:34056200-34066200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:34057800-34058800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:34057800-34058800	Enhancers	Liver	Liver
6	chr11:34057800-34058800	Enhancers	Fetal Intestine Small	intestine
7	chr11:34057800-34059400	Enhancers	Fetal Intestine Large	intestine

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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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