Tag | Content |
---|
EnhancerAtlas ID | HS077-00775 |
Organism | Homo sapiens |
Tissue/cell | H128 |
Coordinate | chr1:151445270-151446620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:151446297-151446318 | TCCTACTTTCTTTTTCTCTCT | + | 6.59 | Myod1 | MA0499.1 | chr1:151445937-151445950 | GGGGACAGCTGGA | - | 6.02 |
|
| 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 |
GH01I151472 | chr1 | 151444981 | 151446490 |
|
Enhancer Sequence | CTTTCTTCCA TCATTCCGTC CTCTCCTTCC TTCTTAATAC TGCTTGTCAA ACTGATTTTG 60 CCACCCAGTT TGAAAAAGAA GGTCTAGAGG ATTATCCCAA TCATTAACTA TTTCTGCAGG 120 TTAGCTTACC TTTCCAGAAT ACAGAATAGA ATTCAGCAAA CTGCCTCAAA GAGCAGTTTC 180 TAGATTTGAC TTCTTCCTCT AGGGTTTATG AAGTCATCAT ACTGAAGTGA CCTGGATTTC 240 CCTATACGTG AACCTCATGA CGTGGGAGCC CGGGGTAGGG AGGGACAGAT AACATGAGAA 300 TCAATAGAAA GAACTGCAAG GTCTGAAGAC AAGAACCATT TGTCTAGTGG AGTCTATTTT 360 ATATCCATTT TTTAAAAATC TCCATTTAAG ATATTTAGCT TCAACGTGCA CCTTGACCAA 420 TTAATCCAAC AAACAAAACT CTGGCTTGGG GGCCCAGTTA CTCACTTTCA TGGAAAGAGA 480 CCTCTGTTTT TAGAACCAGG GATCTTGTGA GTCCCTCCCA CGTCCCCAGC CCTTCTCTGG 540 CCTCGGGTAA CTTTTCCCTC CAGTTTGGTG GAAGGTTACA TTAGAAGAAA ATAGTCCCTA 600 CCGTCTAGAA AGTTTTCGGG GGGGGAAAAA AGGGCGTTGG ACGTGCGGGT GGGTGGGTAT 660 ACCGGGAGGG GACAGCTGGA GCCGCGAAGG CGCGGGGGCC CGCGGCGCGT GGGTGTGGAG 720 GCCGCGGGGC GGCAGGAGGC ACTGGGAAGC GGGGTGAAGA GCACCGAAGT CCAGAAAAGG 780 GCAGTGTCCG CCCTGCGCTC CTCTGCTGGC GCCCGCAACC CGGGAGGGAG CGGCGAGGCT 840 CCGAAGGGTG GGATTCGAGG TCTGAACCCT CGAGTGGGCT TGGGTTTTCA GGAGCCGCCT 900 TTTCTTATTG ATCATTTCTC TTTTGTCATC ATAATCTCTT GGCCTCAGAC TGAGTTAAGG 960 GAGCCATAGT AGGAGTGCAG AAAATGAAGT GGAGGAAAAA AAAATGTGAT ATTTAAAATA 1020 TAGTTTTTCC TACTTTCTTT TTCTCTCTCA AATTAATTTA GATGTAAATA ACATTTTAAC 1080 AGGGCCCAAC ATCAGGCTCC TAGGCTCTGG CTGCTGGTCT CACTTGACAC CAGAATAAGA 1140 TTTTGGTGTG CTAGTAATTT TGCCAAATGG AGGCCTACTC CCCAAAACAT CACCGTGGTG 1200 CATGATGAAC ATTTCTGTAG GTGATGACGT GGAGTTTTTG TTTTACTTCA TTCTAATACA 1260 TGTCCCTGCT TCAAGTGGGT AAAATTATAC CTAGCTCAGC CCAGGTTTAA TTCAGATTAT 1320 TTAAAAAATT TCAGTGGCAA GTAATTTACG 1350
|