Tag | Content |
---|
EnhancerAtlas ID | HS133-09611 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:93696910-93698190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr14:93697902-93697916 | ACTCCCCAGGGATT | + | 6.15 | KLF16 | MA0741.1 | chr14:93697069-93697080 | GGGGGCGTGGC | - | 6.62 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I093230 | chr14 | 93697233 | 93698576 |
|
Enhancer Sequence | GCATGGCTCA GGTAAGAGGA GGTGGGGGGA AGGAGTGCGC TGGAGGGCGG CTCAGGTGAG 60 AGGAGGGGGC GGAAAGTGGC CCCGAGGAGA ACACGTTAAG GCTGACCCGC AGGACTCAGG 120 CACACCGAGC CACGGGAGGC TGGGGACCAC AGGTACCACG GGGGCGTGGC TGTCTTCAGT 180 CTCCCAAAGC TGAAGATGGA CACACTGTTT ATGGGTTGAG TTGGGCGGGG AGGATGGGTC 240 GCAGCTGGGC ATGGTGAGAC GGCTGCCACC TATGGAAGCT GGGCCATCCT GGCAGGGGAG 300 CAAGGAGGCC AGAGTTCCAG AGGAGGACCA GGGAGAGGCT CTGGACAGGA GGCGATCCGG 360 CCTGAGAGCG GGCAGTGAGG TTAGCATTTC AAAGATGGAG ATATTCTGGG GACAGGGGAG 420 AGCTGTGCCA TGGACAGGTA GCTGGAGACG GTCTAGGCAG CTACCAGGAT GACACCAGGG 480 ATTGGAGGGA GAGGATGTTA GGTTGGAGCC AAAGCCTTCA GGATACGAAA GGAGTGACTG 540 GGGGTGGCAG CTGCAAAGGT GGGAGCGGGA CACTGGGCCG TGGGGGCTGG AGAGGTGCTG 600 GGGTGTTAGA GACGTCACCC GCCGCCCTTC CTGACACAGA GTCCGTGGAA AGAGCGAGAA 660 GGAGCCCACG TCCTGGGAGA GGGCTAAGTG GGCGAGGAGG AGCTAGGAGG GCAGCCAGGA 720 CAGGAGGCAG GAGGGGAGGG GTAGGAGCAC AAGGACGCTG GCACTGGGGG GCAGGGAGGA 780 CACCCTGAGC AGGCTGGAGA AACAACCGTG GGTGCGATCA GGGGACTTCT GTAGGAAGAA 840 GGCTGGCGAA TGACTCGGGA GAGCGGGATT GGCAGGCACA GGGTCACCTG ACTGCAACTC 900 TGCAAAGAGC CCAGTCCCAT CAGCCCCGGG AATGGTGGGA TGCTGGGGGC ACTGAGTTCT 960 CTCGGGATCA CTTACAGCTG GACTTCCCAG GGACTCCCCA GGGATTTCAG TGGCTCCGTT 1020 GGAACATGGA GAGATGGGAA GAACAATTGC TTTTAGTTCA GTCTCAGAGG GCAGGGAGGC 1080 ATTTATGGTG CATCTGCTAG AACAGGGGGC CCACGGTACC GTCCATGGCC CGTTAGGATC 1140 GGCGCCACAC AGCAGTAGGT GCGCGGCGAG AGTTATCGCC TGAGCTCCGC CTCCTGCTAG 1200 ATCCGCGGCA GAATTAGATT CTCACAGGAG AACTCTATTG AGAACTGCGC ATGCGAGGGA 1260 TCTAGGTTGC GTGCTCCTTA 1280
|