Tag | Content |
---|
EnhancerAtlas ID | HS049-00015 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr1:2574340-2575540 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:2574921-2574932 | GCTTCCCGCCC | - | 6.02 | INSM1 | MA0155.1 | chr1:2574927-2574939 | CGCCCCCTGCCA | - | 6.07 | KLF5 | MA0599.1 | chr1:2574671-2574681 | GGGGCGGGGC | - | 6.02 | NRF1 | MA0506.1 | chr1:2574631-2574642 | CGCGCAGGCGC | - | 6.14 | PPARG | MA0066.1 | chr1:2575050-2575070 | CTAGGTCCCGATAACCCAAT | + | 6.2 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 2574343 | 2574764 | chr1 | 2574810 | 2575479 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I002640 | chr1 | 2572379 | 2575568 |
|
Enhancer Sequence | GCTGTGAGCG GCGCTGAGCA GGGCAGGGGC TCGAAACCCC GTCCCTCGCC TGCGGTGCGG 60 CCCGCGGGAC CGCCCCTCTC CGGGCGGAGG CACCTGACCC CGACCCGTAG TTCACGGCCC 120 GGGGTGGTAG TGAAGCCTCG GCCCGCGCAG GACCCGCACA TTTGGGCCGG GTCCATGGCA 180 GCAGGAGGGC GAGGCCCCGA GCAGCTGTCG GACCCCGGGA GCCCCCAGGC CGCCCCAGTG 240 GGGAAGGGCG CTCAATCCGA CCCCAGACTC CCCTGAGCCC GCGGCTCGGG CCGCGCAGGC 300 GCAGTGCCAC CCGGAGGGGG CCGCCTGCCG AGGGGCGGGG CGCAGGAAGC GGGGCGAAAC 360 CACTGTTGGC TCATTTCCGG GTGGGTCCCC GTCTCCAGGC AACCATTTCG CGTCCTGCAG 420 ATTCTTGCCT GTGCCGGGAG CCGCCTCCTG GCGCCGCAGC CCAGCCGTAT TCTGCAGCCT 480 CGGAGACCCG CGTCCAGCCC CGCCTCCGGG CTCGGTGACC CCCGTTCAGG AGACCCCATC 540 TAGCCGCCTC CTCTGGGCTC CGGGACCATG GCCCCAGCCA GGCTTCCCGC CCCCTGCCAG 600 GCCCTGCTCC CACCTCGAAG ACCCCAGCAC AGACCCCTCC TCCTGGCTTG GAAACGCCCA 660 GTCCCTCTGG GAGCTCTGAG ACCCCACCCC GCCCAGCCCG GCCGCCTCCT CTAGGTCCCG 720 ATAACCCAAT CTCAGCGTTG CTCTTCAGCT CGGGGGGGGC AGCGGCGCCC CCTCTGCAGC 780 ACCGAACTGC CCCTTACACT GGTGTAGCCC CGACTCCGCC ATGAGCTCCC TGTTCTTCCT 840 AGTGTGGTTT CTGTTTTCCT AAGTGGCCCC GGAGTGCTAG AACCCGCTGG TGTCAGGAAG 900 CATTAAGGAG GTGAAATCCT GCCCAGGCCC CACTGGGGTG TAGTTCTGCC TCTGGGACCC 960 CAAAGCCTGC TGTGCTCTTG GCCTCCCAGC CTGCCTTGTC CCCACGTGCC TTCTCCCGGC 1020 CTGCCATGGG TTTGGGGTGG GCTTCCTGCC GGGCAAGGTG CCCCTGGCTG GCTCAGTCTG 1080 GCCCTGAGGG CAAGGTCCTC TTCCCTCTCT TGCACCCAAG TCACCTGTGG CTTATACTTC 1140 CCATACAAAG AGGCTGAGAG GTCGGTGGGG TTGTAGGGCT AAGGTGGCCA GAGACCGTCT 1200
|