| Tag | Content |
|---|
EnhancerAtlas ID | HS048-15615 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr17:25782820-25783980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:25783007-25783026 | TTCCCACTAGATGGCAGCC | + | 6.12 | | TP63 | MA0525.2 | chr17:25783396-25783414 | TACAAGTCCCAGCATGCC | - | 6.12 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCTGTCCCCC GTGTCTGGGC TGGCTTGGTG GGCTGGGAAT GGCGGGGGAA TGGGACACTT 60
ATTTTGGCAG GTAAATGTGG TTCAGAAGAA AGCTCTTCGT CTTTCTCCAA GCCTGAGCAA 120
TCGTTTTGGC GCAGGCAGTC CAGAGTAGAG CGCTTTGTGA GCCAGCTACA GAAGTGCTGT 180
AAGCCCCTTC CCACTAGATG GCAGCCCCTA AACCCACATA CAAATCCTGG AACCTCCCTG 240
GTCCCCATCT TCCAGGGCTG GGCTGCAGCT GAGGAACTGC GGGACGCACA CCCGCCGGGC 300
GTCCAGGGGG CGCCGCCCCA TCCGGGGGTC GCGGGAAGCT CCTAGGCCGG GTGGGGGACG 360
GAGGCGGACG GGGAGACGCT GCTCCCCCGA CTCTCGGCGC CTGGGGGAGG AGCTGGCGCG 420
GAGCAGCTCC ACCCGGGGCT CCCGGTTGGG GCCGGCCCTC ACCGCCTGCC TCGCCGCGGC 480
CGCCGGGAGG GGAGGGGAGA GGAGGGCAGG GAGGGCGGCG CGGGCGCGGT CCGGGGCCCC 540
GAGGGCGGAG GCCGGCGGCA GGTGCGCGGC GTGGACTACA AGTCCCAGCA TGCCCGGCCG 600
CCCTGACCCA GCCCCCGCCG CCGCTTAAAG GCTCCGGGAG CCGCAGCCGT CGGGTCGCCG 660
CGGCTTTCGC TTTGCTGCCG CGGCTGGGAG GGTGGAAGCG GCAGACTCAG CGGCCGGCTC 720
TACCGGCGTC CCGGCTCGGG CAGCGCCGAG GGGCGCTCCT GGTCCAGCTC TCCTGGCTCG 780
GGGGTTCCTT GCCGAGGCGC CCGCGCCCCG GGCTCCCAGC CTCGGCCGCC GCGGCCCCGA 840
TGCCGAGGCA TGGATAGAGC AGCGCTGCGC GCGGCGGCGA TGGGAGAGAA GAAGGAGGGC 900
GGTGGCGGGG GGGATGCGGC GGCCGCGGAG GGAGGCGCAG GGGCCGCGGC CAGCCGGGCG 960
CTGCAGCAGT GCGGGCAGCT CCAGAAGCTC ATCGACATCT CCATCGGCAG CCTGCGCGGG 1020
CTGCGCACCA AGTGCGCTGT GTCCAACGAC CTCACCCAGC AGGAGATACG GACCCTGGAG 1080
GTAAGTGGGT CGGGGACCAG GCTGGGCTCG AGGAGCGGGC CCGGACACCT CCCTCCGGGC 1140
CCCAGTACTC CTGGCCGAGT 1160
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