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EnhancerAtlas ID | HS037-03428 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr1:225687750-225688690 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr1:225688517-225688527 | ACCGGAAGTG | + | 6.02 | ERG | MA0474.2 | chr1:225688517-225688527 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr1:225688517-225688527 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr1:225688517-225688527 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr1:225688517-225688527 | ACCGGAAGTG | + | 6.02 | MYC | MA0147.3 | chr1:225687843-225687855 | GGCCACGTGCTC | + | 6.92 | Sox6 | MA0515.1 | chr1:225688403-225688413 | CCATTGTTTT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCATGTTTTG AAGCGTGTGG AAGTGCTCTA TTTTAAAATA TTTTTCAAGA AAGCCATATT 60 CAGTACACGG CAAAACAAGG CTTGATTTTC AATGGCCACG TGCTCCCCTT TAAAATTTTA 120 TAACTCAATT TAACTTTTCC AATAGCTTTG CAGTATGAAA ATTCAGTTTA TCTAAAAAAT 180 GTACTTCACC TCTTCTGTGA ATAAGGTATT TTAAATCACA ATCTTATCAC TTACTACTTT 240 TTCCTGAGTA CATAGGTATT AACTATAAGG CATATGAATC CAAACGTGGA CAGTATCTTT 300 TTCTTTTTTA TAAAATTGAG ATAACTGTAC ACATTTGTTT TGTTACCTAA CACAGGCAAC 360 TGTTCACAAT TTACTATTAA GCATACTAAA TTATGATCCC TTGAAGCCTA CAGAGCCTCT 420 ACTCCACCCA CTATACATTT GTATACTTCC ATAATATTTT CTTTAAATAA ATTCCTGGAA 480 TTCATATCAC AGAATTCAAG GTAAGACATT TATTTTTCAG GCTTTTGATT CTGTTTTTCC 540 AAACTGCTTT TTAGAAAGCA GAAGTATAGA AGAGTGCCTG TTTCCTTGCA CTCTTGCCAA 600 AATCAGATTT GTTGGGTTCA ATTTTGCCAA GACAGTCACT GAAAAGTAAA AGCCCATTGT 660 TTTCTTTACA ACTGCGTACC ATGCACTTAC ATTTACACCT TATGCTGTTA TCACTGAACC 720 ACAACCCCAC CCTCCACTAC CTCTGGACCT TCATGCAAAC TCAATGAACC GGAAGTGTAG 780 ATTTGCAAAA ATGCAGTACT ACTAATGCCA CTGTTTAATT TGTATAACAA TAGCTCTATC 840 GTCTTTCTAA GTACATTCAG GATCCATGTC AAAGATATGC ATATGGGATA TTTTTTAAAA 900 AGAAACAAGT ACAAATAAAG GAAAGCTGCC ACTGAGCACC 940
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