Variant report

Variant	rs10912493
Chromosome Location	chr1:172883233-172883234
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172879400-172884200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:172880000-172883800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:172882200-172885800	Weak transcription	Aorta	Aorta
4	chr1:172882600-172885200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:172882800-172883600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:172882800-172883800	Weak transcription	HSMMtube	muscle
7	chr1:172882800-172889400	Enhancers	HUVEC	blood vessel
8	chr1:172883000-172883400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:172883000-172883400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:172883000-172883600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:172883000-172883600	Weak transcription	A549	lung
12	chr1:172883000-172884000	Weak transcription	HSMM	muscle
13	chr1:172883000-172884400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:172883000-172884400	Weak transcription	NHEK	skin
15	chr1:172883000-172889600	Enhancers	NHLF	lung
16	chr1:172883200-172884600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:172883200-172885000	Enhancers	Colon Smooth Muscle	Colon

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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