| Tag | Content |
|---|
EnhancerAtlas ID | HS175-11869 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr17:74822570-74823360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr17:74822931-74822941 | ACCGGAAGTG | + | 6.02 | | ELK4 | MA0076.2 | chr17:74822931-74822942 | ACCGGAAGTGG | - | 6.32 | | ERG | MA0474.2 | chr17:74822931-74822941 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr17:74822931-74822941 | ACCGGAAGTG | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr17:74823117-74823135 | TCTTCCTTCCTTTTTTCC | - | 7.41 | | FEV | MA0156.2 | chr17:74822931-74822941 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr17:74822931-74822941 | ACCGGAAGTG | + | 6.02 | | Gabpa | MA0062.2 | chr17:74822932-74822943 | CCGGAAGTGGA | + | 6.32 | | LMX1B | MA0703.2 | chr17:74822817-74822828 | TTAATTAAAAC | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTTCTCTCC CCCACTCTGC GCTGAGGATG GGCTGGGGAG GAAACGAGGC CTGAAGGCGT 60
CCAGGCTCCG GGATGTCTCC CTCTGCACCG GTCTCATCAT TTCGGTGCAG ATTGAGGTTT 120
CTTCTTGTGA AGGCTGTTAA CAACCAAGTG AGAGCCGGGC TATCAAATGC CGAGTAATAA 180
GATGCCTGTA CCTGCTGCTT CCTGGCCGGA GTGATGGTGC ATTTCTGCTG CTGAAATTGC 240
ATGTGGATTA ATTAAAACGG GAGTAAGTAT TTCTCCTGAA TTATTCACCA GCTTCCAGGA 300
GATGGAACCA TCACTGTGGC GTCTTGTTAC AGGAGTGCTG TGGCCTCTCC TCTGGTGGAG 360
CACCGGAAGT GGAAGGCACG CTCCCGGGGC TGGGGCGTGC ATGTAGGGGG TGCGGTGAAG 420
CTGATCAGTT CTGTGGCTTT GAATCCTTGC ATATCCGGAA GTCACAGAGA ATTGGAAATG 480
CCCTGCACGG GAGAGGCCAG CGGAATAACC CTCTAGAAAG TTCTCCTGCA GAGAAGTAGG 540
AGCCTCCTCT TCCTTCCTTT TTTCCACTGA CGAGGGCCTG CACTCCGCAG GGAGGCCTCA 600
GGAGACTCGG TTTCCATCCT GCCTCTGGTC GGGGCAGTGG CCTCTCCATG CCTGATGGCA 660
GGTCTGGGCT GAGCAAGGGG CCCCTAGGTG TCCCAGTGGT GCTTGTGGGC TGTTCTTGTA 720
TCTGACTGTG GAGTGTCAGA GTGTGTGTTC CATGCCCGCC TGGCCCTTGT GTGGGTATTT 780
GTGGGTGCCT 790
|
| |
|
|
|
