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EnhancerAtlas ID | HS180-04670 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:225688110-225688690 | 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 | TGTTCACAAT TTACTATTAA GCATACTAAA TTATGATCCC TTGAAGCCTA CAGAGCCTCT 60 ACTCCACCCA CTATACATTT GTATACTTCC ATAATATTTT CTTTAAATAA ATTCCTGGAA 120 TTCATATCAC AGAATTCAAG GTAAGACATT TATTTTTCAG GCTTTTGATT CTGTTTTTCC 180 AAACTGCTTT TTAGAAAGCA GAAGTATAGA AGAGTGCCTG TTTCCTTGCA CTCTTGCCAA 240 AATCAGATTT GTTGGGTTCA ATTTTGCCAA GACAGTCACT GAAAAGTAAA AGCCCATTGT 300 TTTCTTTACA ACTGCGTACC ATGCACTTAC ATTTACACCT TATGCTGTTA TCACTGAACC 360 ACAACCCCAC CCTCCACTAC CTCTGGACCT TCATGCAAAC TCAATGAACC GGAAGTGTAG 420 ATTTGCAAAA ATGCAGTACT ACTAATGCCA CTGTTTAATT TGTATAACAA TAGCTCTATC 480 GTCTTTCTAA GTACATTCAG GATCCATGTC AAAGATATGC ATATGGGATA TTTTTTAAAA 540 AGAAACAAGT ACAAATAAAG GAAAGCTGCC ACTGAGCACC 580
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