| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14096 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr16:23812120-23812970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:23812913-23812932 | CTTCCACCAGGGGGCAGAC | + | 6.46 |
| | | 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 |
| GH16I023801 | chr16 | 23812821 | 23812990 |
| Enhancer Sequence | CTTGATTTCA GATTTCTTGC CTCCAAAACT GAAACATACT TTATTATTTA TTTATTTATT 60
TATTTTGTAG AGATAGGGTC TTGCTATGTT GCCCAGGCTG GTCTTGAATT CCTGGGCTCA 120
AGTGATCCTC CTGCCTCCAA TTCCCAAAGC ACTGGGATTA CAGGTGTGAG CCACTGTGCC 180
TAGCTCTTTT TTTTTTTTTT GAAATGGGGT CTCCCTCTGT CGCCCAGGCT GGAGTGCAGT 240
GGTGCAATCT CAGCCCACTG CCACCTCTGC CTCCTGGGCT CAAGCGATTC TCCTGCCTCA 300
GCCTCTCAAG TAGCTGAGAT TCCAGGTGCC CTCCACGACG CCTGGCTAAT TTTTGTATTT 360
TTAGTAGAGA TCAAGTTTCT CCACATTGGC CAGGCTGGTT TTGAACTCCC GATCTCAAGT 420
GATTGGCCTG CTTTGGCCTC CCAAAGTACT GGGATTACAG GCGTGAACCA CAGCGACCGA 480
CTGGCTCAGC TCATTTTTTA AAAACCACCC AGTTTGTGTG ACTTTGTTAA GGCAGCCCTA 540
AGAAACCCAA ACACATGTCA AAGTTTCAAA ACTCGTAGGT AGCAGAGCTG GAATTTGAAC 600
TCAGGTAGGT GTGACCCTAA GGCCAATGCA TTTAAACGAA CAGGATCTAT CTATTTTCTT 660
TTTTGAGCGA ACCCCTGTAT ATAGTGCTTA GCCTGTGCCA GGCTCTAGGC TAAGCATTGG 720
CATGTATCTC TCTGAAACTG GCATTTCGCC TTCTGGGCAG TGCAGTAATT TCCTCCTTGA 780
GGTTGTCTGG TGGCTTCCAC CAGGGGGCAG ACCTGGGCTT TCGTGCACAG GCAGGAAAAT 840
AACACACAAG 850
|
| |
|
|
|
