| Tag | Content |
|---|
EnhancerAtlas ID | HS105-36869 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr18:19315190-19316150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr18:19315697-19315713 | CACAGTGTAAACAAAG | + | 6 | | RELA | MA0107.1 | chr18:19315340-19315350 | GGAAATTCCC | - | 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 |
| GH18I021735 | chr18 | 19315071 | 19316448 |
|
Enhancer Sequence | CGGAGGGCAT TGTCTCACTC AGGAAGCACA AGGGGTCAGT GGATCTCCCT CCCCAAGCCA 60
AGGGAAGCTG TGAGAGACTG TACTGGGAGG AACGGGGTAC TCCGGATCAG ATACTGTGCT 120
TTTCCCACAG TCTTCACAAC CAGCAGACCA GGAAATTCCC TCCGGTGCCT ACGCCACCAG 180
GGCCCTGGGT TTCAAGCACA AAACTGGGTG GTCATTTGGG CAGATACTGA GCTAGCTGCA 240
AGGGTTTTTT TTTTTTTTCA TACCCCGGTG GCATCTGGAA CACCAGCAAG ACAGAACCGT 300
TCACTCGCCT GGAAAGGGGG CTGAAGCCAG TGAGCCAAGT GGTCTGGCTC AGCGGGTCCC 360
ATCCCCACAG AGCCCAGCAA GCTAAGATCC ACTGGCTTGA AATTCTCGCT GCTAGCACAG 420
CAGTCTGAGG TTGACCTGAG ATGCTCAAGC TTGGTCGGGG GGAGGGGCAT CCGCCATTGC 480
TGAGGCTTGC GTAGGCAGTT TTACTCTCAC AGTGTAAACA AAGCTGCCGG AAGTTCGAAC 540
TGGGTGGAGG CCCTCTGCAA CTCAGCAATG ACACTGCAGC CAGACTGCCT CTCTAGATTC 600
CTCCTCTCTG GGCAGGGCAT CTCTGAAAAA AAGGCAGCAG CCCCAGTCAG GCACTTATAG 660
ATAAAACCCC CACCTCCCTG GGACAGAGTA TCTGGGGGAA GGGGCAGTTG TGGGTACAGC 720
TTCAGCTTAC TTAAACGTCC CTGTCTGACA CCTGTGAAGA GAGCAGTGGA TCTCCCAGCA 780
CAGCGTTCGA GCTCTGATAA GGGACAGACT GCTTCCTCAA GTGGGTCCTT GACCCCCATG 840
TATCCTAACA GGGAGACACC TCCCAGTAGG GGCCGACAGA CACCTCATAC AGGAGAGCAC 900
TGGCTGGCAT CTGGCAGGTG CCCCTCTGGG ATGGAGCTTC CAGAGGAAGG AACAGACAGC 960
|
