Variant report

Variant	rs7712774
Chromosome Location	chr5:151148531-151148532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
G3BP1	TF binding region
ENSG00000213433	TF binding region
ENSG00000213433	Chromatin interaction
ENSG00000177556	Chromatin interaction

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151138800-151149600	Weak transcription	Aorta	Aorta
2	chr5:151138800-151149800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:151139000-151148800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr5:151139200-151149600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:151139400-151149800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:151139400-151149800	Weak transcription	Right Atrium	heart
7	chr5:151143200-151149800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:151145600-151150000	Weak transcription	Pancreas	Pancrea
9	chr5:151145800-151149600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:151145800-151150000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:151146000-151149800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:151147200-151149800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr5:151147400-151149000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:151147600-151148600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:151148000-151148600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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