| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14509 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:139649960-139650970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr9:139650074-139650085 | CTTGAGTGGTT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTGTGGCCT TCAAGAGCCG GCCATGGCGT TGGGGGAGAC GTCTGAGGGG GACGGACCTC 60
GAAGGCCAGG GTCTGCAGGG TCTAACTCCA TCCTGCCCCC ACCCAGTCCC AGCACTTGAG 120
TGGTTGGAGA CACTACAGAA GCTTTTGAAG GATGATCCAG TGTGTTGGTG GGAGAATGGG 180
AAGGTCTGGG GCATGAAATG TGCAGGGAAC AGCATGGGGA ACAGTGCAGG GAACCCTGCA 240
GGGAACAGCA TGGGGAACGG TGCAGGAAAC AGCATGGGGA ACAGTGCAGG GAACAGCATG 300
GGGAACAGTG CAGGGAACAG TGCAGGGAAT GCATGGGGAA CGGCACAGAG AAAAGTGCAG 360
GGAACAGCAT GGGGAATAGT GCAGGGAGCA GTGCGGGGAA CAGTGCAGGG AGCATTGCAG 420
GGAACAGCAT GGGGAACAGT GCAGGGAACA GTGCAGGGAA TGCATGGGGA ACGGCACAGA 480
GAAAAGTGCA GGGAACAGCA TGGGGAATAG TGCAGGAAAC AGCATGGGGA ACAGTGCAGG 540
GAGCAGTGCG GGGAACAGTG CAGGGAGCAT TGCAGGGAAC AGCATGGGGA ACAGTGCAGG 600
GAACAGCATG GGGAACAGCG CAGGGAACAG CATGTGGAAC AGCGCAGGGA ACAGCATGAG 660
GAACAGTGCA GGGAACAGCA TGGGGAACAG CGCAGGGAAC AGCATGGGGA ACAGTGCAGG 720
GAACAGTGCA GGGAACGCAT GGGGAATGGC GCAGAGAAAA GTGCAGGGAA CAGCATGGGG 780
AATAGTGCAG GAAACAGCAT GTGGAACAGT GCAGGGAGCA GTGCAGGGAA CAACATGGGG 840
AACAGCACAG GGAATAGTTC AGGGAACAGC ATGGGGAACA GTGCAGGGAA CAGCACAGAG 900
AACAGTGCAG GGAACAGCAT GGGGAACAGT GCAGGGAACA GCATGGGGAA CAATAAGGCC 960
TAGCTGTGTG CACAGCCGGG TTCCACCTGC CATCACAGGG CAACTGCACT 1010
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