Variant report

Variant	rs12092442
Chromosome Location	chr1:214733720-214733721
allele	A/G
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	chr1:214731800-214735000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:214732000-214737200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:214732000-214739400	Weak transcription	NHEK	skin
4	chr1:214732000-214739800	Weak transcription	HMEC	breast
5	chr1:214732000-214740200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:214732200-214733800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:214732200-214736000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:214732200-214738600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:214732200-214739000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:214732200-214739000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:214732800-214733800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:214732800-214734000	Weak transcription	A549	lung
13	chr1:214732800-214737200	Weak transcription	NHLF	lung
14	chr1:214732800-214737600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:214733000-214737200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:214733000-214737200	Weak transcription	NHDF-Ad	bronchial
17	chr1:214733400-214733800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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