Variant report

Variant	rs1069
Chromosome Location	chr17:59574598-59574599
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59564800-59576000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:59572200-59574800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr17:59572400-59574800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr17:59572400-59576400	Enhancers	HepG2	liver
5	chr17:59573000-59575000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr17:59573400-59574600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr17:59574000-59574800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr17:59574000-59577000	Weak transcription	Hela-S3	cervix
9	chr17:59574200-59574800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr17:59574200-59577200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr17:59574200-59581400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

Quick Search:

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

what's new

Quick links