Variant report

Variant	rs13414750
Chromosome Location	chr2:210408729-210408730
allele	A/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	chr2:210407400-210409200	Weak transcription	Fetal Brain Female	brain
2	chr2:210407400-210412200	Weak transcription	Brain Germinal Matrix	brain
3	chr2:210407400-210413000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:210407800-210409200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:210408400-210411800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:210408600-210412600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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