Variant report

Variant	rs58563692
Chromosome Location	chr19:41959677-41959678
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41955600-41960000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr19:41955600-41962600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr19:41955800-41960000	Weak transcription	HUVEC	blood vessel
4	chr19:41955800-41961200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr19:41955800-41962200	Weak transcription	Fetal Intestine Small	intestine
6	chr19:41955800-41962400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr19:41955800-41962400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr19:41955800-41963000	Weak transcription	Fetal Intestine Large	intestine
9	chr19:41956000-41961600	Weak transcription	Left Ventricle	heart
10	chr19:41958800-41961600	Weak transcription	Spleen	Spleen
11	chr19:41959400-41960600	Enhancers	Primary B cells from peripheral blood	blood
12	chr19:41959600-41959800	Enhancers	GM12878-XiMat	blood
13	chr19:41959600-41961200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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