Tag | Content |
---|
EnhancerAtlas ID | HS047-14162 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr17:25790190-25791680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr17:25791370-25791382 | GTCTGTTTACTT | - | 6.52 | FOXP2 | MA0593.1 | chr17:25791371-25791382 | TCTGTTTACTT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTTATCCAT TTGCCACTGC ATCTGTAATC ACACTGACGG CCAAGAGTTT AAAAGGAGGC 60 TGGGCCTGGG TGCGGTGGCT CATGCCTGTA ATCCCAGCAC CTTGAGAGGC TGAGGCTGGT 120 GGATAGCTTG AGTCTAGGAG TTCGAAACCA GCCTGGGCAA CATGGTAAAC CCCGTCTCTA 180 CAAGAAATAG AAAATTAGCC ATGCATGGTG GCACGCTCCT GTAGTTCTAG CTACTCAGGA 240 GGCTGAGGTG GAGGTTGCAG TGACCTGAGA TTGCATCATT GCACTCCAGC CTGGATGACA 300 GAGAAAAAAA AAAAAAAAAA GAGGCTGGAC ATGGTCCTCT GGCTGAGATT CTGGGATAAG 360 TGTCAGGAAC TATGGCTTCT AGTTTTGTGG TTGCTTGTGT CTGAGGTTCT GGGCTATGTG 420 TCAGGCATTG TGGCTTCTAG TTTTTGTGGT TACCTGCAGC AAAGGGGGGC CCCCTGGGCT 480 GACCAATTAG AAGAAGGCCT TTTCCTTGCT CCAAGATAGC GGAGGGAGGG GCTGGATTTC 540 AGGTCTCCCT GTCCAGAGAC TGATCAGCTT TGGTAGTACA TAATCATATG GTGAGGTCTT 600 GATCACTTGA GGCTCATGAA AGTCACTTTA ACTGCATTCT TGGTTGCATC CCTAACTACA 660 AATACTGATC ACAGTGCTAT TTGGGGTGCC TGGCTTTGGG GATGATTTAG TAGAGTTGTG 720 GGTTCCTAGG GCTACAAAGG GTCTTGGAAT TTCCATGTGG TCCAGCCCTC TCATCTTGCA 780 GGTGAGGAAA CTGAAGGCCT GAGGGAGAAC TGACTTGCCA GGAACCCCTG TTAAGCAGAA 840 TTAACAAAGG GTGGTTATTA AAGGAGCACT GAGTTGGGAG TCAGACCTGG AGGCCCACAC 900 CCTTGATTAA GACATTATAC CACCTTGAGT CTGGCCTGTT GACTGAGGGT GAGCCACTCC 960 ATCCTCCTCT GATTGTGGGG TGTTGACCTC AAGGGGTTTC CTGCAGGAAG AAGCAAATGG 1020 GTTTGCTTTC CTAGCTCTGT CCCAGTGCCT TAGGGGCCCT GAGGACTGGA GAGATTCTTG 1080 GAGCGCCATC TGGGGTATGT CACGGGTGGA CCTTTTTTGA AGGTCAGTCT GCTCAGTGGG 1140 CTGGCTCAGC CCGAATGAAC TGTCTTGAAT CTTTGGAGTT GTCTGTTTAC TTTTAAGGGC 1200 TTCTCATCCT TGCACCAAAA GATCCCCTGG AAATTAGGTG GGAAATCCTT AACTTTTATG 1260 GGGCCTTGTG TTTGTCTTAA AAGTTCATGC GCATGGCCAG GTGTGGTGGC TCACACCTGT 1320 AATCCTATCC TGGATCCCTT GAGTCAAGGA GTTTGAGACC AATGTGAACA ACATAGTGAG 1380 ACCCTGTCTC TACAAAAAAT AAAATATTAG CCAGGGGTGG TTGTGCACAC CTGTTGTCCC 1440 AGCTACTACA GTGGCTGAGG CTGGAGGAGC ACTTGAGCCT GCACTGAGCT 1490
|
| |
|
|
|