| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11352 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:16439670-16440590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr17:16439780-16439792 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:16439784-16439796 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:16439788-16439800 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:16439792-16439804 | 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 |
| GH17I016535 | chr17 | 16438315 | 16440715 |
|
Enhancer Sequence | ACTCGGGAGG CTGTGGCAGG AGAATCGCTT GAACCGAGGA GGCAGAGGTT GCAGTGAGCC 60
GACATCGCGC CACTGCACTC CAGCATGGCG ACAAAGCGAG ACTACGTCTC AAACAAACAA 120
ACAAACAAAC AAACAAAAAA AACAAAAAGA AAAGGAAAAA AAAGGGTGGC CAATATAGTG 180
AAACCCCCTC TCTACTAAAA ATACAAAAAT TAGCTGGGCG TGGTGGCGCG CGCCTGTAGT 240
CCCAGCTACT CGGGAGGCTG AGGCAGAAGA ATCGCTTGAA GCCGGGAGGC AAAGGTTGCA 300
GTGACCCGAG ATTGCGCTAC TGCACTCCAG CCTGGGCGAC AGAGCGAGGT TCCGTCTCGA 360
AAAAAAAAAC AACGAAAAGG GGACTCACTT CGGAGAAGCT GCCCTCTCTG CAAACTTATT 420
TGAGTAAGGG ACTGAAGACT GAAGTTAGGG AGAGGAAAGG GATACACGTC TGTTAGTGCG 480
AGTTGCGTGT CTTGTTAGTG CGAACTGGAA CCCAAGTTTC CTTTGGGAAG ACTTTGGCGA 540
AAGAGTACAG GAACACCAGC CACTCCAGAA AGAGACCGCT CCTCTTGAAC CCGCCCACTT 600
AACTCCTCCC GCAGGCTCTA CGTTCGAATG CCTCCACCCT GATTTTAGAA GGTTATAGGC 660
GCACAATCAA GGAAATGTCG ACAGAGGGCG TCCTTGCTCT AAGCAGCATT GTCCACCTGC 720
TTCCTGAGCG GGGTTCAGTG ATTATTCTCT GAACCTGGAC TTCTGGCGTT GTGCCTCTAT 780
ACTCCATTTC CCTGCTTCAA AGCTCTCCTA ATTGACTTTA TTTTCTGACA CTCCCCCACT 840
TTACCCCCCA GGAGTGTTGC TTCTTTTATT TCTTTGCCTG GATGGTCGTT TGGCTTAGTA 900
AATAGACCTA GACCCCACCC 920
|
