| Tag | Content |
|---|
EnhancerAtlas ID | HS047-15788 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:21012620-21013670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr18:21012650-21012671 | AAAAAAAAAAAGAAAGAGAAG | - | 6.22 | | NKX2-3 | MA0672.1 | chr18:21013119-21013129 | TTCAAGTGGT | - | 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 |
| GH18I023433 | chr18 | 21013441 | 21013610 |
|
Enhancer Sequence | GGAGACAGAG TGAGACTCCT TCTCAAAAAA AAAAAAAAAA AGAAAGAGAA GGAGCAATTT 60
GGGAGCCATT GACGCCTGTA ATTCCAGCAC TTTGGGAGGC CAAGGCGGGA GCCCAGGAGT 120
TGAAGACCAG CCTGGGCGAC ATGGTGAGAC CCTATCTTGA CAAAAAATAC AAAAATTAGC 180
CGGACATGGT TGTGCAAGCT GTGCTCCCAG CTACTTGGGA GGCTGAGGTG GGAGGATCAC 240
TTAAGCATGG GAGGCAGAGG TTGCAGTGGG CCAAGATCAT ACCACTGCAC TCCAGCCTTG 300
GCAACAGAGC AAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAAATTGG AGCCATTGAA 360
AGGCATGCAA GCAAATTTCT TATGCTTATT ATCCACTTGT AACTCTTTTC TTTTTTTTTT 420
TTGAGATGGA GTCTTGCTCT GTCACCCAGG CTGGAATGTA ATGATGCAAT CTTGGCTCAC 480
TGCAACCTTT GCCTCCCAGT TCAAGTGGTG TTCCTGCCTC AGCCTCCCAA GTAGCCATGA 540
CTACAGGCAC GCACCACCAT GCCCAGCTAA TTTTTGGCTA CTCTCGAACT CCTGACCTCA 600
GATGATCCAC CTGTCTTGGT CTCTCAAAGT GCTGGGATTA CAGGCATGAG CCACTGTGCC 660
TGGCCTTGTA TCTCTTTTTT CAGTGAATTG TCTACTTCTG CTGTTTACCC ATTTATTTTC 720
ACTGAGGTTT TAGTATTTAT TAATTTAATA AATTCTTTGT ATTTTACAGA TGCCAACCAC 780
TTGTCCAGAA CAGAAATGAA CTTTGCCTCT GAGCTGAAGG CTCAATTGCT ATGAGGGGAA 840
GAAGGACAGC TGGCTGCCTA GGGCCTGATT ACAGCTGGAA CCTCCCAAAG GATGGAGGAA 900
CACGTCATCA GCCAGGGCCA GCCCAGGCCA CCAAGCCAGA GCTCAAGGGT GTGGTGCTTT 960
CTCCTCCCTC CCTACCTAGG GCAGCTTCCT TTGACAGCAC ACTTGCTGCT TCAAACTTCT 1020
AACAAATATC GACCATTCTT TCAAACAATA 1050
|
