| Tag | Content |
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EnhancerAtlas ID | HS050-66051 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr8:59182950-59183830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr8:59183351-59183361 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr8:59183351-59183361 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr8:59183351-59183361 | ATTTTCCATT | + | 6.02 | | ONECUT1 | MA0679.1 | chr8:59183503-59183517 | AATATTGATTTTTG | - | 6.83 | | ONECUT2 | MA0756.1 | chr8:59183503-59183517 | AATATTGATTTTTG | - | 6.61 | | ONECUT3 | MA0757.1 | chr8:59183503-59183517 | AATATTGATTTTTG | - | 6.74 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGCATTCCT ATTATATGTA TGTTTTCTTG TTTTATCCAG TCTAACAGGA CACTGTTAAT 60
TTCCCATAAT CAGGTTTTTC ACCTTGGACA ATCTTTATTG CTCTATATTT GAGTTCACTT 120
ACTCTTTCTC TGTTCTATTT GACCATTAAG TTTTTCCACC GACTTTTTAT CATAATTATA 180
AATTTTAGTT CTATAACTTC CAGTTGTTTC CTATTTTATT GTTTTTAATT TTCTGCTGAC 240
ATTTCCAACT TCTCTGCCAA GATTTCTATT CACTGAAATC ATGTTCTGTT TTATTTCATT 300
GACTATTGTT ATAACAGCTG TCTTAATTTC TTTATCTGTC AGTTCCAGCA TCTGGTTCAT 360
CTCTAGCTTG AACACAATTA ATGTTTTTTT CTCCTTAGAA TATTTTCCAT TTTCTTGGAT 420
CTTTACATGT TGGATAATTT TGGACAGAAC GTTAGTATCA TGGATGTTAA CAGATCCTAG 480
ATACTGTTAT TTTTATCTGA TAGAGCATTT TTTTTTCTTT TTGCAGGTAA TATTCTTAGT 540
TGGTCTTCAA CTGAATATTG ATTTTTGACA GCAGTTCAGT TTCAGTTCAG ATCTTTACCA 600
GAGCTGCTTT GTGTCTTTTC CATGCCATAT GCTTCTGGAT TCAGTCAGTG ATATGATGGA 660
CAGGACCAGG GATCCCCTCT CTGATGATGG ACAGGACCAG GGATCCCCTC TCTGCCTCTT 720
TCCCTTCTAA TATTACCCCA CTCTCTCTCC AACATTTACA ATTTTCTGGC TTCATTTTGA 780
TTTCTCAGAC CAGAAAAATT AAGTTTTCCT AATGGACCAC TGCCACTGCT GTCTGAGCCA 840
TGAAGACAAC ACTTAGCCCA GGCTAAAAGC AGTGGAGTTG 880
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