Variant report

Variant	rs2248939
Chromosome Location	chr12:104816193-104816194
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	chr12:104808600-104816200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:104808800-104824200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:104811000-104817200	Weak transcription	Fetal Thymus	thymus
4	chr12:104814800-104816600	Enhancers	Hela-S3	cervix
5	chr12:104815200-104816600	Weak transcription	NHEK	skin
6	chr12:104815200-104817400	Weak transcription	Thymus	Thymus
7	chr12:104815400-104820200	Weak transcription	HMEC	breast
8	chr12:104816000-104816200	Enhancers	Aorta	Aorta
9	chr12:104816000-104816200	Enhancers	Placenta	Placenta
10	chr12:104816000-104817000	Enhancers	HSMMtube	muscle
11	chr12:104816000-104818000	Weak transcription	Gastric	stomach

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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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