| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17382 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:117571750-117572560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr12:117571981-117571991 | ACCATATGGC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I117133 | chr12 | 117571692 | 117572356 |
|
Enhancer Sequence | GGGTATCTTG GTTTCCACTA CACTATTTTT TTTCAATGTT TTGATGTTGC TTAGACGTCT 60
ATTAAAAGAG CACTGTTTAA ATGAACTTTA CAGTAGGGGT GAGGACACTA CAGCCTGTGA 120
GCCTAACCCA ATCCACGGCC TGGCTCTGGA CATAAAGGTT TAAGGAACTC GCTCGTATTG 180
CCTGTGGCTG CTTTCCCGCT ACAATGGCAG AGCTGAGTCA CTGCAACAGA AACCATATGG 240
CCCGCAAAGC CCAAAATACG CACTGTCTGG CCCTTTACAG AAAAAGTGTG CCAACCCCGG 300
CTTCAGAGGA AATCGTATTT TCAGAAGCAA CTTCCTTCAG AAGTCTTTGT AGGCTTAGAA 360
TAGGTTTCCC CCAAACTTCA AGAGCACACG TTACTGAGAT GGTGAAGGAT AACATTTCCT 420
CGCTTTCCTT CTACAAAGTA AATGTGATTG ACAAGAGACA GTGCTGTAAC TGGCCAGGAG 480
GCTGCCATGT ACAGTTAGTG AGAAAGAAAT AACAAAGCTT GGCAGGGCAT GGTGTCTCAC 540
GTCTGTAATC CTAGCACTTT GGGAGGCTGA GGCTGGTGAA TCACTTGAGC CCAGGAGTTT 600
GAGACCAGCC TGGGAAACAC GGCGAAACCC CATGTTTACA AAAAAAAAAA AAATTTAAAA 660
AGTAGCTGGG CATGGTGGCA CATGCCTGTG GTCCCAGCTC CTCAGGAGGA TGAGGCAGGA 720
GGATCACTTC AACCCAGGAG TTTGAGGCTT CAGTGAGGCT TGATGGTGCC ACTGCATTCC 780
TGCTGGGGTG ACAGAGCAAG ACCCTGTCTC 810
|
