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EnhancerAtlas ID | HS080-03207 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:225688070-225688690 | 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 | 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 | ATAACTGTAC ACATTTGTTT TGTTACCTAA CACAGGCAAC TGTTCACAAT TTACTATTAA 60 GCATACTAAA TTATGATCCC TTGAAGCCTA CAGAGCCTCT ACTCCACCCA CTATACATTT 120 GTATACTTCC ATAATATTTT CTTTAAATAA ATTCCTGGAA TTCATATCAC AGAATTCAAG 180 GTAAGACATT TATTTTTCAG GCTTTTGATT CTGTTTTTCC AAACTGCTTT TTAGAAAGCA 240 GAAGTATAGA AGAGTGCCTG TTTCCTTGCA CTCTTGCCAA AATCAGATTT GTTGGGTTCA 300 ATTTTGCCAA GACAGTCACT GAAAAGTAAA AGCCCATTGT TTTCTTTACA ACTGCGTACC 360 ATGCACTTAC ATTTACACCT TATGCTGTTA TCACTGAACC ACAACCCCAC CCTCCACTAC 420 CTCTGGACCT TCATGCAAAC TCAATGAACC GGAAGTGTAG ATTTGCAAAA ATGCAGTACT 480 ACTAATGCCA CTGTTTAATT TGTATAACAA TAGCTCTATC GTCTTTCTAA GTACATTCAG 540 GATCCATGTC AAAGATATGC ATATGGGATA TTTTTTAAAA AGAAACAAGT ACAAATAAAG 600 GAAAGCTGCC ACTGAGCACC 620
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