| Tag | Content |
|---|
EnhancerAtlas ID | HS043-17913 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr17:38108120-38109220 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr17:38109077-38109092 | TGTGGGCGTGGCTGG | - | 6.21 | | SP3 | MA0746.2 | chr17:38109077-38109090 | TGTGGGCGTGGCT | - | 6.37 | | SP4 | MA0685.1 | chr17:38109075-38109092 | GGTGTGGGCGTGGCTGG | - | 6.36 | | SP8 | MA0747.1 | chr17:38109077-38109089 | TGTGGGCGTGGC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTGATCCAC CTGCCTCAGC CTCCCAAAGT GTTGGGATTA CAGGCGTGAG CCACCACACC 60
TGGCCACAGT GCCCCATTTC TGACCTTCAC AGACATCCCC CATCCAAGAA CAAGAAGCTG 120
AAAATGCCCT CAGAAGGTCA GAGAAGCAGA GGGCTCTTCT CCCCATCCCC AACCCAAAGG 180
TGGACAAAAC CTTAGAAGGT GAGAGGGACA CAGAGACCCC TTTCCTAAGC AAAGGAAAGA 240
AATCTGTCAA GTCAGCAGCT GAAGCCCAGA GCCCCTTCGC AAGGGAAAGA CTTTGGGGTG 300
ATGGTGGGTG GGATGCAGAG GGGTCCCCTG GACATTGGCG GGACGTAGTG CTGACTGTGA 360
TGGCAGCCAC GGGTTTCTTG GGCCTTTTCG GTGCATCCTC CCCGCAAGCC TCCACCACGC 420
TGTTCCAGGT AGGCTGAGGT TAGGCCCACT CAGGGCGGCA CCTTGGCGCA GGACACCTCT 480
TCCGTTTGGG CTTTCCGTCC TCGTGATTTC GCTCTCCATC TGACAGTCAT CCATGGTGAC 540
AGGGTGTGTC CCTTTCCCCT AAACAGGATC CTCAATGCCC ATCGGAAAAC GTTGTAAGGC 600
GTTGAGCCCC CAACGCCCCC TCACCACAAG ACCCTGCTGT GACCATCTTT TCCTGGTGAG 660
GAGAGTCTGC ACGGGGGAGC AGGGCGCCAT ACCCCAGAAA GAAACCTCTG TGCCTGGGAG 720
TGAGGGACTC GCTGAGTAAA GTGAGGTCGA AGAGGGTGGA GAGGGGTAGG GTCCCAGTCA 780
CCACTGTCCT GAACCCACAG TTCAGTCCGG GCCCAAGATG GCCCCACAGG AGCACAGGGG 840
GTTTCGGGCG CTGCAGGTGG AGGTGAAGGA CCAGCTGCGG TGCGGAAAGG CCTGACCCGG 900
GCGGCAGATC GCCTGCGGAG AGAATGACCG GCTGGGGTGG AGGCGGGGCT GGGGTGGTGT 960
GGGCGTGGCT GGGGAGGCGT GGCTGGTGTG GTAGGCTTAA GCAGTGAGGG CGGGACTGGG 1020
GCAGAGGCGG GGTTTGGGCG CTGAGGGCGG GGCTGGGGCT TTGAGGAGGT GGCTGGGGCT 1080
GGGGCGAGGC TGGTGCGGAG 1100
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