| Tag | Content |
|---|
EnhancerAtlas ID | HS129-22589 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr20:42297880-42298800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr20:42298749-42298761 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr20:42298753-42298765 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr20:42298757-42298769 | AAACAAACAAAC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTCTCCCCC ACTTGGCCTC CCAAAGTGTC GGGATTACAG GTGTGAGCCA CCTTGCCTGG 60
CGCCATCCTG ATTTTTTGTT CAGGAAGAGT TATTCCAGGA GTGACTGCCT CTAGACCACC 120
CCAGGTCCTG GGCTACTTCT CCCATGAGGG GCTCAGTGGA GGAACCCCTC CTGTGTGAAG 180
GATGGCAGCT CCACAGCCCT CAGCCCATTT CCTGGCCACT TGCTGTAACT CTCCTCTGCC 240
CTAGTGCCCC ACTTCCCGCT TTGTCTCTGA CTCACCCCTG TCCTGGAGCA GAGCCCAGCA 300
CGTTGAAGGG CAAAAGGTAG GGTATGTTGG ACCACAATGT GGTTGCCACC ACTAACTGGA 360
CTCTGCTTTT TCAGCTGGGA TTAGGATATG AGGACTTGCA GGTGTCTGGA GTTAGGAAGG 420
TTCAGAGCCT GGCTCTATGA ACTTGGCAGG TGGCCTCACC CCTCTGAGCC TCAATTTCCG 480
CATCTGTTAA GGGGGATAAT GAGAATGTGG GTGAAGTTGA TGGCCAGCAC ATATGGTAAA 540
GTATATCATC TCACAGAAAT GCCCCAGCTG TCTGAGATGC TGACCCTATC AAACAGCATT 600
GGAGGCTGGG TGTGGTAGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGAGTTCA 660
AGACCAGCTT GACCAATATG GTGAAACTCC TCGTCTCTAC CAAAAATACA AAAATTAGCC 720
GGGCGTGGTG GTAGGCGCCT GTAAGCGCGG CTATTCGGGA GGCTGAGGCA GGAGAATTCA 780
CTTGAACCCA GGAGGCAGAG GTTGCTGTGA GTCGAGATCA TGCCACTGCA CTTCAGCCTG 840
GGTGACAAAG CGAGACTCTA TCTCAAAATA AACAAACAAA CAAACAAACA GCATTGGAGC 900
ACCAGGGAGT GTCCATGCAG 920
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