| Tag | Content |
|---|
EnhancerAtlas ID | HS150-09994 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr7:54796050-54796720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr7:54796664-54796675 | CATTGTTTATT | + | 6.02 | | Mecom | MA0029.1 | chr7:54796176-54796190 | AAGAAAAGATAAGC | + | 6 | | NFE2L1 | MA0089.2 | chr7:54796333-54796348 | TGTGCTGAGTCATGC | - | 7.05 | | Nfe2l2 | MA0150.2 | chr7:54796335-54796350 | TGCTGAGTCATGCAA | - | 6.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTCAATAAC TGAGATTGAC TGGGACACCA TCACAAAGAA ACCCCTGTAT GTGTCAACAC 60
TGAGTGTAAT GAAGCATGTG TGAATGCCCT CACAACTGCC AACCACAGTT ACCACTCAGA 120
AGAATGAAGA AAAGATAAGC GATTCAGAAG GCATATCCCC GAGATCCAAA CTGGAAATGC 180
AGGTGAGCAT CAGAAGCAAT TCTAAACAAA GGAAAAAGGA AAACAGTGTT GACCTTCTAA 240
CAATCTTTAT CTCCTAAGAA CGCTGGCCCT TTGTCATGTA ACTTGTGCTG AGTCATGCAA 300
CTGTGCTGCA TCCTCAAGGA GCATCCTCAA GGAGCCAGCC TGGGCTCATG CAGAAGGTGC 360
AGTGCTCCAA GTATTCCAAT GCTGAACTGC ACGTTGTATG GTCTCTTCAG GCCAGGCTCA 420
AAAGTGACAA AGCCTCACTT CACCAAATTA TCTTGTTCAA AGCAATCAGA GCCAGTTCAA 480
ATTCAAATGG AGGGGAAATA GAGTCTATCT TTGGCTGGGA CATACAATGA AGTCATGGGG 540
ACATGCATAT AGGATGAGAG AAATTGTAAT GATCATCTTT GCAAATATTT CCCAGGTTTT 600
CATTTGACTT AGAGCATTGT TTATTTGTTG AATTAGTTAA TATGCCCAAT ATATACCACG 660
CTGTATTTGT 670
|
