Variant report

Variant	rs12371989
Chromosome Location	chr12:106667652-106667653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106661600-106669000	Weak transcription	Psoas Muscle	Psoas
2	chr12:106664000-106668200	Weak transcription	Spleen	Spleen
3	chr12:106664800-106669600	Enhancers	Stomach Mucosa	stomach
4	chr12:106665000-106668400	Weak transcription	Esophagus	oesophagus
5	chr12:106665400-106668200	Enhancers	HepG2	liver
6	chr12:106665600-106669200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr12:106665600-106670200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:106665800-106670800	Weak transcription	Fetal Heart	heart
9	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:106666400-106669600	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr12:106666400-106670600	Weak transcription	NHEK	skin
12	chr12:106666600-106670400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr12:106666800-106670400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr12:106667200-106669400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr12:106667400-106668200	Enhancers	Liver	Liver
16	chr12:106667400-106669000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:106667400-106669600	Enhancers	Pancreas	Pancrea
18	chr12:106667600-106668000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr12:106667600-106670400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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