Variant report

Variant	rs13014614
Chromosome Location	chr2:171684722-171684723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171679600-171688800	Weak transcription	K562	blood
2	chr2:171680200-171688800	Weak transcription	NHDF-Ad	bronchial
3	chr2:171680400-171686800	Weak transcription	Aorta	Aorta
4	chr2:171681200-171693800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:171682200-171691600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:171683400-171688800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:171683600-171685000	Strong transcription	Brain Germinal Matrix	brain
8	chr2:171683600-171694200	Genic enhancers	Cortex derived primary cultured neurospheres	brain

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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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