| Tag | Content |
|---|
EnhancerAtlas ID | HS101-20602 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr18:68082780-68083910 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr18:68083236-68083247 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr18:68083236-68083247 | GGGTGACTCAG | + | 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 |
| GH18I070415 | chr18 | 68082482 | 68083963 |
|
Enhancer Sequence | GTATGTGGGT GAAATTAATG AAAGGATTAA TGAAAGCTAT TGCTATAAAG TTTACATATA 60
TGAAAACAAA GTCATGTTTC TAAGTCACAT GTAAAGACAA TCATGATAAA TACATTTAAA 120
AATCAGCAAC CAATTCTAAA TTAGCTAATT TCAAGGTTAA GAAGTGATGT AGCAGAACTT 180
AGAGCACCCC AAAATAAAAT TATTTTCACT TTACTTTCAA ATTTTAATAC ATTTAATGAG 240
TTGCCTAATC AAGTCAAGCA GAATAATAAA CATTGAGCAG AAAAAGTACA CCTGTTACTA 300
GAATACTTAT TAGTCTGTAT TCAGAGTACT TATAAAATAG AAAGCTGAAA GCATCAGGGT 360
AACAACTCAG CTTCATTTTG TTATTTTTCC CTGCTTAGGT CTTCAGCAAA CTCTTCAACA 420
AAGCAGTCAG GCTGAGGAGG TGAGCCTCTC CCTAGAGGGT GACTCAGGCT GGCGAAGCTC 480
CTGCCCAGGT AACCACACCC CGCAGGAGGC GGGTCTCATC CTGGGCGATG GGGAGCAGGA 540
GGTGATGGTG GTGGTGGTAT TTGAAGTGGT GCTTCATTCC ACTCCAGGTG TGACAGTGAC 600
AGTGATGGTG ACAGTGAAGC AAGGGTAGAA GCGTGTTTTA TAATCAGGGC TGCCAGGTGA 660
TCAGGGAACG GGGAGGGAGA CAGGGCTGTA CAGGGCGGTA GCAGTGAGAA AGGCAAGGGC 720
TTAGGCCGAG GCGGATTTAA AGGAGAACAA CCAGGCCAGG CCAGATGGCT CACATCTGTG 780
ATCCCAGCAC TTTGGGAGGC TGACGCGGGA GTATTGCTTG AGGCCGGGAG TTCAGCCCAG 840
GCAACGTAGT AAGACCTATC TCTACCAAAA AAAAAAAAAA AAAAAAAAAA AATTGGCAGG 900
TGCAATGGTG TGGCCTGTAG TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG GATTACTTGA 960
ACCCAGGAGG TCAAGCCTGC AGTGAGCTAT GATCACGCTA CTGTACTCCA GCCTGGGCAG 1020
CAAAGCAAGA GCCTGTCTAA AAAAAAATAA GATAAAACAA AAGAAAGAAA CAAACACCAG 1080
AAGGCACTCT CAGGCACAGC CTTCCAGTGT GACCTAGTTA GTGCTGGGCT 1130
|
