| Tag | Content |
|---|
EnhancerAtlas ID | HS040-20535 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:111942980-111943720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:111943455-111943467 | AAACAAACAAAC | - | 6.32 |
|
| | 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 |
| GH02I111184 | chr2 | 111942268 | 111944602 |
|
Enhancer Sequence | CAGGTTGAAC AATCTTCTGC CTGACCCGGA GAACACAAAG CAACTCCCTT CTGTTGGCTG 60
TAATGTGTGA ACGCTGAGCA CTTCTCAAAG GCCAAGCACT GAGTTCAATG CTCTCTCAGA 120
TCATTGGATT AATTATTGTC ACAAATTAGC TGGTGGAAGC TCCACTGTTC AGGGGATTTC 180
ACAGAGGAGG ACTCTAAGGT TTAACAACTG ACCCGAGGCA CTTGGCTGGT GGGCAGTGTC 240
TCTGGGCACC TCCCTAGCTG ACTCTCCTAT GCCACCTGCC TCGTGACCGG GCACATGGCC 300
GAAGGGGTGA GTGGGTGCCA AAGGTCGACC TTGAAGCGTG TCACCCGCTC CCTGGGGAAC 360
TAAGTGTTCT GTGTGGGGGC TGAAGTGCAG AGATAATAGT GGAATTTACC TCTCAAGACT 420
GCAGGGCTAA GTGTGACTTT TGTTTGATAA GCTTGGGTTT TATGTCTTTA GGAGCAAACA 480
AACAAACCAT AAAGTGGCAG TCTGTTGGAG TGAGTCCCAG CTGAGCTTGC AGGAAGGGAG 540
AGGCTCTGGG CTCTGCCCCT GGGGAAGAGC GAGAGAGGCA GGCACAGTGC GGGTGGGGGA 600
GACTCATAGA GCTTCCCTTT CCTCATGTGA AAAGTAAATC GGATTCTATG GTAATAACCC 660
AAAGCTCACT TAAAAGGCTC ATTAATGAGG AAAACAATAG CAGTAAGAAC AATGGCTATA 720
TTACACTGAT GCCGTGTGCC 740
|
