| Tag | Content |
|---|
EnhancerAtlas ID | HS101-10805 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:69069920-69070670 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:69070525-69070543 | GGAAGGAAGGAAGGAAGC | + | 10.05 | | EWSR1-FLI1 | MA0149.1 | chr12:69070487-69070505 | GGAAGGAAGGAAGGAAGG | + | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr12:69070491-69070509 | GGAAGGAAGGAAGGAAGG | + | 10.83 | | EWSR1-FLI1 | MA0149.1 | chr12:69070463-69070481 | AGAAGGAAAGAGGGAAGG | + | 6.46 | | EWSR1-FLI1 | MA0149.1 | chr12:69070471-69070489 | AGAGGGAAGGAAGGAGGG | + | 6.84 | | EWSR1-FLI1 | MA0149.1 | chr12:69070517-69070535 | GAAAGACAGGAAGGAAGG | + | 7.02 | | EWSR1-FLI1 | MA0149.1 | chr12:69070533-69070551 | GGAAGGAAGCAAGGAAAA | + | 7.66 | | EWSR1-FLI1 | MA0149.1 | chr12:69070499-69070517 | GGAAGGAAGGTTGGAAGG | + | 7.82 | | EWSR1-FLI1 | MA0149.1 | chr12:69070521-69070539 | GACAGGAAGGAAGGAAGG | + | 7.97 | | EWSR1-FLI1 | MA0149.1 | chr12:69070495-69070513 | GGAAGGAAGGAAGGTTGG | + | 8.38 | | EWSR1-FLI1 | MA0149.1 | chr12:69070467-69070485 | GGAAAGAGGGAAGGAAGG | + | 8.45 | | EWSR1-FLI1 | MA0149.1 | chr12:69070475-69070493 | GGAAGGAAGGAGGGAAGG | + | 9.09 | | EWSR1-FLI1 | MA0149.1 | chr12:69070483-69070501 | GGAGGGAAGGAAGGAAGG | + | 9.47 | | EWSR1-FLI1 | MA0149.1 | chr12:69070529-69070547 | GGAAGGAAGGAAGCAAGG | + | 9.6 | | EWSR1-FLI1 | MA0149.1 | chr12:69070479-69070497 | GGAAGGAGGGAAGGAAGG | + | 9.93 | | FOS | MA0476.1 | chr12:69070120-69070131 | GGTGACTCATT | + | 6.02 | | ZNF263 | MA0528.1 | chr12:69070428-69070449 | AGGGGAGGGCAGGGGAGGGGA | + | 6.14 | | ZNF263 | MA0528.1 | chr12:69070423-69070444 | AGGGGAGGGGAGGGCAGGGGA | + | 6.1 | | ZNF263 | MA0528.1 | chr12:69070438-69070459 | AGGGGAGGGGAAAGGAGAGAA | + | 6.24 | | ZNF263 | MA0528.1 | chr12:69070484-69070505 | GAGGGAAGGAAGGAAGGAAGG | + | 6.24 | | ZNF263 | MA0528.1 | chr12:69070464-69070485 | GAAGGAAAGAGGGAAGGAAGG | + | 6.48 | | ZNF263 | MA0528.1 | chr12:69070468-69070489 | GAAAGAGGGAAGGAAGGAGGG | + | 6.48 | | ZNF263 | MA0528.1 | chr12:69070412-69070433 | TGAGGAAGGGGAGGGGAGGGG | + | 6.65 | | ZNF263 | MA0528.1 | chr12:69070461-69070482 | GGAGAAGGAAAGAGGGAAGGA | + | 6.76 | | ZNF263 | MA0528.1 | chr12:69070488-69070509 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | | ZNF263 | MA0528.1 | chr12:69070413-69070434 | GAGGAAGGGGAGGGGAGGGGA | + | 6 | | ZNF263 | MA0528.1 | chr12:69070472-69070493 | GAGGGAAGGAAGGAGGGAAGG | + | 6 | | ZNF263 | MA0528.1 | chr12:69070476-69070497 | GAAGGAAGGAGGGAAGGAAGG | + | 7.58 | | ZNF263 | MA0528.1 | chr12:69070480-69070501 | GAAGGAGGGAAGGAAGGAAGG | + | 8.12 |
|
| | 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 |
| GH12I068674 | chr12 | 69068697 | 69070990 |
|
Enhancer Sequence | AAAAAACTAG CCGGGTGTGG TGGCGCATGC CTGTAATCCC AGGTACTTAG GAGGCTGAGG 60
CAGGAGAATT GCTTCAACCT GAGAGACAGA GGTTGCAGTG AGCCGAGATC GCGCCACTGC 120
ACTCCAGCCT GAGCAACAAG AGCAAAACTC CGTCTCAAAA AAAAAAAAAA AAAGAAAGAA 180
TAAAACATTG GGCGGGGCAC GGTGACTCAT TCATGCCTGT AATCCCAGCA CTTTGGGAGG 240
CTAAGGCAGG CAGCTTGCTT GAGCTCAGGA ATTTGAGACG AGCTCAGGAT TTCGAGACCA 300
GCCTGGGCAA CAAAGTGAAA CCCAGTGTCT ACAAAAAAAT ACAAAAATTA GCTGGGCATA 360
GTGGTGTGCA CCTGTAGTCC CAGCTACTTG GGAGGTTGAG GTGGGAGGAT CGTTTGAGCC 420
CAGGAGGAGT CGAGGCTACA GTGAGCCATG TTTGCGACAC TGCACTCCAG CCTGAGTGAC 480
ACAGTGAGAT CCTGAGGAAG GGGAGGGGAG GGGAGGGCAG GGGAGGGGAA AGGAGAGAAG 540
GGGAGAAGGA AAGAGGGAAG GAAGGAGGGA AGGAAGGAAG GAAGGAAGGT TGGAAGGGAA 600
AGACAGGAAG GAAGGAAGGA AGCAAGGAAA AAGAAAAGAA AAGAGCATTG TTCAGGCACA 660
AGGCCCTCAA GTTTGGTTTG TTTTTTTTAA AAAAAGAATA AAACATTGAA GAAAGAAAAA 720
AGAAAAGAAA AGAAGGCAAA AGAAAGAAAC 750
|
