Variant report

Variant	rs16947485
Chromosome Location	chr12:117779637-117779638
allele	C/T
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	chr12:117771600-117789000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:117773200-117779800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:117773600-117780000	Weak transcription	NHEK	skin
4	chr12:117773600-117782600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr12:117777200-117785400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:117777400-117785400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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