| Tag | Content |
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EnhancerAtlas ID | HS007-09479 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr2:189315430-189316240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr2:189315998-189316013 | TTGCTGAGTGAGCAT | - | 6.08 | | MAFF | MA0495.3 | chr2:189315998-189316013 | TTGCTGAGTGAGCAT | + | 6.11 | | MAFG | MA0659.1 | chr2:189315995-189316016 | GGATTGCTGAGTGAGCATATT | - | 6.44 | | MAFG | MA0659.1 | chr2:189315995-189316016 | GGATTGCTGAGTGAGCATATT | + | 6.79 | | MAFK | MA0496.2 | chr2:189315996-189316015 | GATTGCTGAGTGAGCATAT | - | 6.48 | | MAFK | MA0496.2 | chr2:189315996-189316015 | GATTGCTGAGTGAGCATAT | + | 6.66 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCTTTTTG AGACAAAGAT GTTTCCCGTT TATTAAGTGC ATTTGTACTT AATAAACTTT 60
CCAAAAGAAT TGCTCTTCTA TAGTTCAGTT TGGGACCCAC AGAAGCAAGA GTAGGATTAC 120
TCCATGTTTC AGGAGCCTCA ACTTTACTAT TCAACAAGGA TTGCAATTCG AGCACCATCT 180
GCTTCACAGC TGAGAATCAT TAAGCTTCAG CAACATTTCC CCATCTCAGC ACCTGACTTC 240
TGCCAAGCAA GTAGGAAGTT TTGCCTTCAC CTTCACCTTT CAGCAAATTA CTCAATTAGT 300
AAATGGGTAT ATGCTACCAT TTAAACTCCA AAATGTAGTG ACTCTTTTTA GCTGAAAACA 360
AACCACCATT GGTATCTAAA TTAACATTGT ATTTTGCTGA TGATTTCTAA ACTTGAATTG 420
TTTTTAAATG CTACTTTTCT ACTTAATTTT TCCTAACAAT TTATGATGTA AAACACATGG 480
TACATTCGGG AGGAAAGCAT GTTGTTTCAC TTTACCTGAC CAATGTTGGC ATGATCAAAG 540
ACATTCACAA ATGTTCACTT TTGTTGGATT GCTGAGTGAG CATATTTGTG TGATGTTAAA 600
GGAATGAGCT TGGGCTGTAT GTTGCCACAT ATGGTTTGCA TTATGATAAA TGAATGTTAA 660
TAGGAAAAAA AAAGTAAAGC ATTGGAAACA TGAGAAAACT CCAGATTTAT TTCTCTTTAA 720
AAGAAAGTTT TTATTTTACA TCTACCAAGA CAGGACATCT TTGTAACAGG GCATATACTA 780
CATTTTTATC ATTAAGTAAT TATTATCTGC 810
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