| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08927 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr13:26760220-26761020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:26760361-26760382 | AAAAGAGAAGTGAAAGCAAGC | - | 6.18 |
| | | 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 |
| GH13I026185 | chr13 | 26759591 | 26762164 |
| Enhancer Sequence | CAGACGATTT ACTCGGGAGT AAGAATTCAG GTCATTCACC AAGGCGCCCA TGTCAAAGCT 60
TCATCACCCG CCTCGCGGCC CTAAAACGTG TCAGAGTCAT GATACACACA ACGCAGAGGA 120
AAAGTTCAAA AACAGATCTT AAAAAGAGAA GTGAAAGCAA GCGATCAAAA CATTTCTGGA 180
AATCTGACAC ATCTGGAGTG CCGTGTGGAG ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT 240
AAAAACCCAG ACCGGGAGGC CAGTGCGTGT GTAAGACCGC GTTTCTCTGC AAGGCTGTCC 300
CGCGGCAGGA ACGCGCTCGT TGGGCCGCAG AGCAAGAGCG GGACGCGCCG GGGGGCGTCT 360
GCGTGGCACG TGGGCCCCGC AGCCAGTCGC GCTACCGACT GGCAGTCAGC GGAGACGCTT 420
CGGAGCAGGT CTGTTAGGGC GCGCGCACAC ACATGCACGT GCACGAGCGC ACGTACACGC 480
GCACACCGCC AGCGCGGACC CTGACGGGGC CGAGCCTCGG AATTGGGCCT CCTCGGCCGC 540
CGTCGTCTTC TCAGCTCTCA CAGGGCCCGC AGCGGCGCTA TACCTTCGGC CACAGGTAGC 600
GCGTTCCTTC GCTGTGCTGA CCGTCGATCC CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG 660
GGCAGGGAAG CGTCAGGGAC CTTTCTTCTT CTTTTTTTTT TTTTCTTTTT TTGAGACGGA 720
GTCTCGTTCT GTCGCCCAGG CTGGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAATTTCC 780
GCCTCCCAGG TTCACGCCAT 800
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