| Tag | Content |
|---|
EnhancerAtlas ID | HS184-22944 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr4:89099370-89099880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr4:89099620-89099635 | CTGTGACTCAGCACA | + | 6.33 | | Nfe2l2 | MA0150.2 | chr4:89099618-89099633 | AGCTGTGACTCAGCA | + | 6.27 |
|
| | 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 |
| GH04I088177 | chr4 | 89098808 | 89100528 |
|
Enhancer Sequence | ACTTCAATAC CAGCTCAACC ACAGTAGAAT AGGGAACCAG TCAGAGTTGT GAGGCCCTAG 60
CTCTTGGATA GCATTTCTAG AAACACCCTG AGCCAGAAGG GAAATTGCTG CCTTGAAGGG 120
AAAAACACAG TCCTGGCAGG ATTTATCACC TGCTGACCAA AGAGCCCTTG GGCCCTCAAC 180
AATCAGTAGC GGTACCCAGG CAGTACTTGT TGTAGGCACG GGGTGAGACT CAGAGACTTG 240
CTGGCTTAAG CTGTGACTCA GCACATTCCT AGCTGTGGTG GCTATGGGGA GGGGCTACTT 300
CTGCTTAAGA AAAGGAGTAC TCTCAAGTGT AATGAAGACT TTGTCTTGCA GCGTAGGTAC 360
CAGCTCAGCA CAGTGAGGTA GAGCACCAAA TGGGCTCTTG GGGTCCCTGA TTCCAGGCCT 420
TGGTTCTTAA ACAATATTTC GGGACCTGCC CTAAGCCAGA GGGGAGCCCA CTGCCTGAAG 480
GGAGAGTCCC AAACCTAGCA GCATTCAATA 510
|
