| Tag | Content |
|---|
EnhancerAtlas ID | HS093-08063 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr12:132662830-132664020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | | Gata1 | MA0035.3 | chr12:132663975-132663986 | TCCTTATCTGT | + | 6.14 | | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 | | ZNF740 | MA0753.2 | chr12:132662876-132662889 | CCGCCCCCCCCAC | + | 7.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 132662941 | 132663228 | | chr12 | 132663524 | 132663727 | | chr12 | 132662936 | 132663290 | | chr12 | 132663332 | 132663875 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132178 | chr12 | 132662746 | 132663750 |
|
Enhancer Sequence | GGAGGGTGGG GAGCCCGGGA GTTTGAGGCT GTACTGAGCT CAGAACCCGC CCCCCCCACC 60
CCCTGCACTC CAGCCTGGGC GACAGAATGA GACCCCTGAA AAGTGTTGGT TTCTGACTTT 120
TTTCGTTTTT GAAATCGTTT CCGGCTGGCC CAAGTCGAAA AATAATGCAG ATGTCTCCAG 180
CTGTCCCTGA GAACACTTCC TGTTCCTTGA TCTGTGGCTT GTGATTCTCC CCCCGCCCCC 240
ACTCCCCTTA CATGGGGCTG TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC CTCAGGATTG 300
TATGACTGCA GGTTGGGCTG TCCCTTGGGA TTCAGGGCCT CAAATGTACC TGCTGACCAG 360
TTGAAGAGTG CTGACCAGCT GTCCTGCTGA ACACCTCTCA ATCTGGATTT TTGACATTTC 420
CCTGTGATTA AATTCAGGGA ATCCAGCTTT GGTGACAGAG CCACTGAAGC AAGGCTGTTC 480
CCTGCTTGGA GACGCACCCA CTTTACACGT GTAGGGTGGC GAGTCTGACA AACGCAGCCA 540
CAGGCAGCCC CCACCGGGGG AGCCGGACGT TTCCATCCAC CCAGACAGCA GCGTTCACGC 600
CCAGGACCAT GTGGGCCTGC GCCCCGGGCC GCACCTGCCT CTCCTGCATT CCGTGTCTGG 660
CATCTTGTGT CGTTGCCACC CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA GCGAGTGTCC 720
TCCGTGTCTC CGAGTCGCGC CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA GAGCTGTTGT 780
TTGTTTAGGG ATGTATCATG TTTTCAGCTT AACATTTGTG CCATTCGTGT GCCCTGGCGA 840
GCCCCGCCCC CTCCAAGTTA CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT ACTCTTCCTG 900
CTGTCGCCAG CGCAGCCGAA GCACCAAGCA GGAAGCTCTG CCGAGTTCTT GGCTTCAGGT 960
AACGTGTCAG ACCCAGGGCA TGAGCTCCAG TCCCTCTTGC CTCCACAAAG GACAGCACAT 1020
TTCCAGTTCA GGGTGCTGTG GCCGACACCG TGCGTGTGGC TGGGGCCAGT GTCACCGCGA 1080
ATCTCGGCTG CTCCACGCCC TTGCTGTGGG CTTGGGGCCA GTGCTTTACC TCTCTGGCCT 1140
CAGTTTCCTT ATCTGTTAAC AGGGTTGGTG TGAGAATGAA TGAGAAGGCA 1190
|
