| Tag | Content |
|---|
EnhancerAtlas ID | HS076-02359 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:50513860-50514820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr1:50514667-50514677 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr1:50514667-50514677 | AACATATGTT | - | 6.02 | | JUN(var.2) | MA0489.1 | chr1:50514744-50514758 | GGAAAATGAGTCAT | + | 6.3 | | MYCN | MA0104.4 | chr1:50513921-50513933 | GGCCACGTGGTC | + | 6.52 | | MYCN | MA0104.4 | chr1:50513921-50513933 | GGCCACGTGGTC | - | 6.52 | | ZIC1 | MA0696.1 | chr1:50514406-50514420 | TACACCCCGCTGTG | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCGCCTCGGC GCAGGCCCCG CACCCCCGAC TCTGCCCGCC CTCTGTTACG GACACCCGCT 60
GGGCCACGTG GTCGCGACTG GCTTCTCCCA GCGGCCAGCC TGGCCACCCC GACTCCCAGG 120
GAGGGGGAGA GGGCCCTTGC AAGAGGATCC TGCCCCCGCG CTGCCCAGAC CTGAGGGCTC 180
CTGGCGACCC CACCCGCAGC CCATCTGGCG GCTCTGGCCC CGCAGGTCAG GGTCACACCC 240
CTGCCGGCCT CCTGAGACTT CCCGGCCCCA GGGGAGAGAG CTGAAACTTG GGTTGACGCG 300
CGCCCCCTCC CCAGCGACAG GCGACCCCGC AGCAGCCCCG CGCCACTCCT CTCTGCGCCT 360
TTCCGTAGTT GTCCTCGAGG TGGCTTTGTT GAACGTCCTG GTGGCGCCAA AAAGTCCAGG 420
CAGCTTCGGG CGATCAGGGT CCCGAGGCGC TGGGCGCGCG GACTTGGATC CTCAGGGGGC 480
CCCTCTGTGT GACTTTCGCT AATTGTCTCA CAGGGAGGGC AGCACCCTCC CCTATCTTTC 540
CTCTATTACA CCCCGCTGTG GACCTGGGAC TTGGGTATTT CTAGACGAGA TTGGGAAGGC 600
GCGTGTGTTA CACTAAGCAG TGCTCATGTT TAGCTGAGGA AGAAGGAGCC TCAAGTGTTC 660
GTAGGGTGTA CCTGTGTATG TTGTAATTGT TGTCTCTCTT TGGGCTGGGG GCTGTTATAC 720
ATGTAGGATT TAGTAAACAC AGGTCTTGAA GTCTTGAACC TGCAGGAGAC TCATTTGTTT 780
CTACAAGGAG AGAACCTCCC CTCCCCCAAC ATATGTTAAG GGACTTGAGG AGACCACAGG 840
GAAACCGAAG GGAGGGACTT CTAGAAAACA ATTCCAGGTT TGGGGGAAAA TGAGTCATAT 900
TGATTCCCAA GCTGTTAGCC AATACCACTC AAGGGTAATA ATTTTCATAA AATCTTCCCA 960
|
