Variant report

Variant	rs10839952
Chromosome Location	chr11:7983486-7983487
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:7969800-7985800	Weak transcription	HSMMtube	muscle
2	chr11:7980800-7986800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:7981600-7984200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:7982200-7983600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:7982200-7984600	Weak transcription	Pancreas	Pancrea
6	chr11:7982400-7985200	Weak transcription	Osteobl	bone
7	chr11:7982400-7986000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr11:7983000-7983600	ZNF genes & repeats	HSMM	muscle
9	chr11:7983200-7984200	Weak transcription	Placenta	Placenta
10	chr11:7983200-7984400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:7983200-7990800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:7983400-7985800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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

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