| Tag | Content |
|---|
EnhancerAtlas ID | HS045-52129 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr5:489050-490270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:489355-489373 | GCCTCCTTGCTGCCTTCC | - | 6.22 | | Esrra | MA0592.2 | chr5:489831-489842 | TTCAAGGTCAT | + | 6.62 | | Esrrg | MA0643.1 | chr5:489832-489842 | TCAAGGTCAT | + | 6.02 | | MAX | MA0058.3 | chr5:490016-490026 | ACCACGTGCT | + | 6.02 | | MYCN | MA0104.4 | chr5:489296-489308 | GGCCACGTGGCC | + | 7.22 | | MYCN | MA0104.4 | chr5:489296-489308 | GGCCACGTGGCC | - | 7.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGGGGATG AGCAGGGCTG CGGTGGGAGC AAGGGGGCCC GGAAGACGTG GGTCCATGTG 60
GTCCCTAGCT CCCGGCCGGC TTCCCTCCCC GCATCTGCCT GTGGGCTCTG GTGCCCCTCG 120
CTGGGGAGGT TTTACTGAAA TGCAGCCTTA TCCTTCACAA GTCTTTGCCA TTCAACCCAG 180
GGTTCAGGCC TCGAGGAGGC CACGTGGGGG TGCCAGGCTC CAGGGGACCC TCAGGGAACT 240
GAGTGTGGCC ACGTGGCCCC GAGAGTCTGC CCTCTCTCAC GGCCGCAGGG CTCAGAGGAC 300
ACTGGGCCTC CTTGCTGCCT TCCCGGCCGT GAGGGTCCAG GGACCAGGAG ACGCCAGGGC 360
CGTGAGGGTG TGGGAGAGAC CACCCAGGGA GGGGGAGGCC CCCGACGAGT CCCCCCGCAC 420
AGCTGCTGCC TCTCTGCTGG GCTGGAGCGG AGCCCACCAC CCCTCTGGGC TGAGGCTCGG 480
GCTGAGGAGG GGTTTGTCCC TGGAGCCGGA CGGGCCCCAG GAGACAGCAG AGAGCAGCCT 540
GGCCAGGGGT TTCTGTGCTG GCGCCTGGGA GGGGACAGAT CAGGGTCATC TCTGCGGTGA 600
CTAAACCCCG AGTTTGCTGT GAGCTCCTAA GCCCCAGCAG CCTCTGGCCA GTGTCACAAC 660
ACCCCGAGGA AGTGACAGAT GCCAGAAGAA CCAGCGTTCA GGGAGTTAAA GTTCCATGTT 720
GGAACGGGAA CCACACAAGC CTTCTCCTCT TCCAAACTCA GGCCTCAGGA CACGAATCCC 780
CTTCAAGGTC ATCTTTAAAC GCGGCCTCCT GGCACGGCCG CCCCCAGGGC AGTGATGGCC 840
CCCATGGATG TCCTGGGGTC GGCCGCGTTC AGACTCCCCG GCCGGCAGCC TTCCCGTCTG 900
GACAGTTGCC CACGGCCGTG CCAGGAGGGC TCATGCCACC AGACCGCATG TTCCAGGCCT 960
TTCTCCACCA CGTGCTTTGC CTGTGCAAGG GCCTCTGATG CCTGAAGCTC TCGCAGGGCC 1020
TGTCCCCACA CTGCCCGGAC AGCCCCCGGG CCAGCACTGC CATGTCGACC CTTTCCCATG 1080
GGGCACGTTT GGCCTTGAGA CGCTCCACAG GGCTTGGCCT CTGGTCTGCA GAGATCAGTT 1140
GCAGCCTCCC AGCTCTCTTG GACTCCCAGG AATGGGATGG ACCTGCCGGC CATGGGCATC 1200
TCTGTTCCAG AACCTCAGGC 1220
|
| |
|
|
|
