| Tag | Content |
|---|
EnhancerAtlas ID | HS045-27286 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr17:27396600-27397380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EHF | MA0598.2 | chr17:27396690-27396702 | TATTTCCGGGTT | - | 6.04 | | ELF3 | MA0640.1 | chr17:27396689-27396702 | TTATTTCCGGGTT | - | 6.21 | | MYC | MA0147.3 | chr17:27396854-27396866 | GGCCACGTGCGC | + | 6.32 | | POU2F2 | MA0507.1 | chr17:27396879-27396892 | ATATGCAAATATA | - | 6.3 | | SOX10 | MA0442.2 | chr17:27397308-27397319 | TGCTTTGTTTT | - | 6.02 | | STAT3 | MA0144.2 | chr17:27396807-27396818 | CTTCTGGGAAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63416 | chr17:27369672-27424111 | NCI-H69 |
|
| | 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 |
| GH17I029069 | chr17 | 27396701 | 27396890 |
|
Enhancer Sequence | GGGTAGGAAG GGGCCTGTCA GTCCCAGTCA CTGACTCTGG GCCTCAGCTC AGGCCAGAGT 60
TCCAAGGGCC CTTAAAAGGG CGGGAAACAT TATTTCCGGG TTGCTCGGAG AGTAGACCTG 120
TCCTAATGCC GCTGTAATCA TTAAAAGGGC AACACAGATG GGCTGCCCAT CGGCGGCTTG 180
AAAACCCATT TCTTTTAAGG GGAGTGGCTT CTGGGAAGTG CGTAAAGAAC CTCCAGGCAG 240
GGGCGGGACC AGAGGGCCAC GTGCGCCAAT GAAAAGTGGA TATGCAAATA TATATATGAA 300
TATGCTAACG AGCTCTCGGT TTCCCAGTGA ATGGTAGGGC ACAAGCCTGG ACTGGCAGAG 360
CGGGCTAGGG AAGAAGAGGA AATGAGAGGA CCTCGAGGTT CAACCGAGTG TCTGAATGGA 420
AACTAACTCC CGACAGACCA TGCACAACGT TTCTTCCACA GCACCCGGAT CTCGAAGCCC 480
CACTGGGCAT CAACTGTCAG TCCCTCACTA GGGGGGATGA AGGGGGAGGG CGTGGGAGAT 540
TCTTTTGGCT GTGGTAAGGA GCTCTGAATT TAGAAGCCAG AAGGTTCTTG CCAGCAATAC 600
TACCTTGTTT CACAGATGGG GAAACTGAGG CCTGACAGGT TAAGCCCCTT CTCCAAGGTC 660
GCAGTGCTAG ACGCAGAAGA ACTCAGTTTG GCAGGTTTTG TCTATTTTTG CTTTGTTTTC 720
ATTACTGCAC GGGGGCACCA CTCTGGAGGT GAAAAGGCAG CAGCCTGAAA GGCGGCAGAG 780
|
