| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04422 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr13:25268010-25268580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:25268398-25268417 | ATGCCAGTAGGTGGCACTG | + | 6.93 | | KLF4 | MA0039.3 | chr13:25268196-25268207 | CCACACCCTCC | + | 6.32 | | MLX | MA0663.1 | chr13:25268455-25268465 | ATCACGTGAT | + | 6.02 | | MLX | MA0663.1 | chr13:25268455-25268465 | ATCACGTGAT | - | 6.02 | | MLXIPL | MA0664.1 | chr13:25268455-25268465 | ATCACGTGAT | + | 6.02 | | MLXIPL | MA0664.1 | chr13:25268455-25268465 | ATCACGTGAT | - | 6.02 |
|
| | 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 |
| GH13I024694 | chr13 | 25268139 | 25268490 |
|
Enhancer Sequence | GGCTGATTGG AATTAAACCT CTTTGATTCC GGTTTATCCC TCCTGGGGTC TTTCTCGAAT 60
GCCACTAATT TCCCTTAATG GTGCTTTTAT AGTCACTTAA CTTTGCTCAA AATCTCTCCG 120
TACTTCCCTG TTTTCTGCTT CTCAAGTCTA GACCTCAGGC TACCTTTCAG GGCCCTCCAG 180
GTCTTGCCAC ACCCTCCACA TCCGCTTGTA CCTTGAACAC TCACGGACGA GCCTGCCCCT 240
CATGCCCCTG CACCCGCATC CTGGTTTCTG GAAGGCTTTC TTCTCTGTGT ATCGGTAACC 300
CACCTATCTA TCAAGATCTA GTTCGTAGCT GCTTTTTTCC ACGAAATCTT CAGTCCTCGC 360
AGAGGTCCAG CTTCTCCAAA CATCCCTAAT GCCAGTAGGT GGCACTGTTG TTTACACGCT 420
TACCACGGTC TTGCGGCCCT CCCTGATCAC GTGATAATGT CTCTCCAGCT AGGTGGTAAT 480
GGGATCAGGA GGGTGTGTTT TGGGTCCTAT GCTGAGGGCA TGTTGGTTCA TTAAATATGT 540
GCTGCAAATA TTTTTCTTCT TTGATTCCCA 570
|
