Variant report

Variant	rs73871864
Chromosome Location	chr3:143611237-143611238
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143603600-143616800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:143610400-143611600	Enhancers	Fetal Stomach	stomach
3	chr3:143611000-143611400	Active TSS	Stomach Smooth Muscle	stomach
4	chr3:143611000-143611600	Enhancers	Fetal Muscle Leg	muscle
5	chr3:143611000-143612000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:143611000-143612400	Enhancers	Fetal Thymus	thymus
7	chr3:143611200-143611800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:143611200-143612000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:143611200-143616400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	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

what's new

Quick links