| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01307 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr1:37055990-37057180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:37056588-37056606 | GGAAGGGAGGAGGGCAGT | + | 6.21 | | EWSR1-FLI1 | MA0149.1 | chr1:37056152-37056170 | AATCCCTTCCTTTCTTCC | - | 6.26 | | IRF1 | MA0050.2 | chr1:37056349-37056370 | TTATTGTTTCACTTTCAGGTA | + | 6.15 | | ZNF263 | MA0528.1 | chr1:37056573-37056594 | GGGGAAGGGGATGGAGGAAGG | + | 6.15 | | ZNF263 | MA0528.1 | chr1:37056578-37056599 | AGGGGATGGAGGAAGGGAGGA | + | 6.17 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGAAGAGC CGGGACAGGG CTGGGAATGT GCAGCCTCCA AGGGCCCCTT GACAGTGTCG 60
CTATGGAGGT ATTCAAGGTT ACATTGTTAC TTCTCTGGGA CACACACCCA CTCAAGGCCT 120
GGCCAGAGGG GCGGGCTCAT TTGTGTGGTT CATTAGGGGA TGAATCCCTT CCTTTCTTCC 180
CCTATGGGCT GGGCTTCAGA GTCCCTTTCT CTGTACTTTT TGCTGCCTTA TCCCACAGAA 240
TCCTGGATTT GGCAGGGTAA CTGATACAAT GAAAAACGGC AAATTGCAAC TTCGGGGTGT 300
AAACAAAATG CAGCATTATT TGTTTCTCCC ACTGTGCTTT TGCATTTTAT CCTCATGGCT 360
TATTGTTTCA CTTTCAGGTA AGAAGGCCAT TAAAAAGTCA CTTTTAGGCA TAAAATAGGT 420
TTCAATTACA AAATAAGGAT GTATAGTCCC AGACGATAAT CCACATTTCA CATCTGATTT 480
AAAGTCGAAT CTTTTCCCTC TTGTGGAGGG AATCTGGCTT GTGACCAGAA CAGCTGACAG 540
ATTGCAGGGG ACAGGGCATG CTGTAACTGA GTCCTCCAGG GCTGGGGAAG GGGATGGAGG 600
AAGGGAGGAG GGCAGTGAAC TTCCTTTCTC ATTCATTCTT GGGTGCTGAC TGACGATACG 660
CATCTCCGTC CGTTTCCCCT CAGCTTCCAC GTCTCTAATG GGCCCTCTCC ACACAGACTG 720
TTGCTGTTGA GTCCCAGCTC TTCCTGGAAG TCCCCGTGGG CATGACTCAA AATGGTCCCG 780
AGCTGTTCTC TTTCTGGGCT CAGCAGTGAG CACACAGCCT TTGTCCCCTC ATGCACTGGG 840
CATGCAGACA CCCCCAGGGC AGCTGCTTCT CTTCTGCCAT AGTCTCTTGC CTATGGTAGG 900
AGTTAGACCC CAGGATGGAG TCTTAGTCAG GCCCCACACT TCATTAGGCA CTGTCTGTTG 960
CATCTTGGTG CCTCCGTGAA AACTTCTTTT TAAAATCCCA ACGCGTTACA TGTGTCAGAG 1020
GACAGTTCCG CCTCCTGCCT ACGACAGAGG GTTGGTAACA GGGTGTCCAG AACCAGCCAT 1080
ATCCAGCTGC CTGTGGCGCC CCCCTCAGCC CTTCCCTGCA CATTGGCCAT CAGGCAATAA 1140
GACTGATAGG AAATTGTCAA TCTGAGTAAA CTATAGAATA TCGAACCCCA 1190
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