| Tag | Content |
|---|
EnhancerAtlas ID | HS040-15572 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:45005390-45005880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr17:45005600-45005612 | TGCCCGAGGGCA | - | 6.27 | | TFAP2C | MA0524.2 | chr17:45005600-45005612 | TGCCCGAGGGCA | + | 6.52 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28004 | chr17:44999703-45009235 | Fetal_Intestine | | SE_29222 | chr17:44999726-45009313 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 45005698 | 45005789 | | chr17 | 45005565 | 45005619 |
|
Enhancer Sequence | TTCAGGTGTC GGCTACCTCA GGCTGCATTC CTACATCAGC CCCCATACCT CCACACCCCC 60
GCATCATCCC ACAATATCCC AGACTTACTT TCCGGAAGCA ACGGCCTGGT CTCGGACTCT 120
AGCAGTGATT TCTAGTTGCT TCTCAGGGCC ACAGGTCTTG CCTAGGAGCA CCCTGGGGAG 180
TCATTTGACA GCTCACCCAG CTTCTTTTGG TGCCCGAGGG CATATCTGGA GGCCATAGGG 240
AAGCCCTGGA AAAGACTGGG CACAAGCTGA AGCCAAAGTT GGGTGCCTGG CTGGCATTGG 300
TAGATTTGGG GTCCTGGTTT GCATTGCTCA CGATGCAGAA TGGTTGCTGA CCTTTCCTCC 360
AGCGTTGGGG ATGATGTGAG AGTCCAGCAG GCCCCCTTCA TGTGGGCCCT AACTTGGGGA 420
AATCTCCACC GTGAGCACCG GGAAGTGGAT GGTGGGGCCA GCATAAGCAG TATCCCGAGG 480
ACTGATCATG 490
|
