Variant report

Variant	rs73195700
Chromosome Location	chr12:106671852-106671853
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:106669600-106672800	Weak transcription	Liver	Liver
3	chr12:106669600-106673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr12:106670400-106673000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr12:106670400-106673200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:106670800-106672800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr12:106671200-106673200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr12:106671400-106672000	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr12:106671400-106674800	Weak transcription	Stomach Mucosa	stomach
10	chr12:106671600-106672200	Enhancers	HepG2	liver
11	chr12:106671800-106672200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr12:106671800-106674000	Weak transcription	Fetal Heart	heart

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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