Tag | Content |
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EnhancerAtlas ID | HS180-39865 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:138708800-138709990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr5:138709390-138709404 | AGTCCCTAGGGAAG | - | 6.13 | RELA | MA0107.1 | chr5:138709285-138709295 | GGGAATTTCC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I139372 | chr5 | 138708591 | 138710125 |
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Enhancer Sequence | GCTAAATAAA ATCTTTGGAG GTAGGGATAC ACCAAATAAT TTGTTTTTTT GTGTTGTGTT 60 TTTTTTGTTG TTGTTGTTGT TTTTGAGACA GAGTCTTGCT CTGTTGCCCA GGATGGAGTA 120 CAGTGGGTTG ATCTCGGTTC ACTGCAACCT CTGCCTCCCA GATGCAAGCG ATTCTCCTGC 180 CTCAGCCTCC CGAGTAGCTG GGATTACAGG TGTGACCCAC CACGCCCGGC TAATTACTGT 240 AATTTTAATA GAGATGAGGT TTCACCATGT TGGCCAGGCA CTGGTGTCGA ACTCCTGACC 300 TCAAGTGATC AGCCCGCCTT GGCCTTGCAA AGTTCTGGGA TTATAGGTGT GAGCCACTGA 360 GCCGGGCTAG TAATTTTTAC AACTAGGAAT TCTCCCTCAG GTGGGGCAGG GTCACATGAG 420 ATCTCAGGTT TTCACAAGAG GGCTGGGATC GACAAAGACT GAAATACTAT AAATCTAGCA 480 GGAGTGGGAA TTTCCACTTG CTGGCAGCCC AGGCTGAGAA CAAACCCATG AGTAGCACAA 540 ACCAAGTTAT GTTCCAAAAT CTCACAGGAG AGGGCACTGA GGGAAGGTGG AGTCCCTAGG 600 GAAGACTACC TGGAAGAGAC ACTGTTTGGG CTTGGCTCTA CAAAGGGCAC ACACAGTCTG 660 GAAGAGAAAC CTTGATTGGG CTTGGCTGTA CAAAGGGCAC ACACAGTGGG CACAGTAGAG 720 TGGGATGAGC CATAGGTGTG GCGTAGGACT ATGTTTCTGG TGTCCGATTA CCTCGCACCA 780 CTGCCAAGAC ACACATGGCA GCCAGCCCAG AGCTCCCTCT AGCAGACCAG TCAGCCTGCC 840 CACTACATCC CAACCTTCAG TGCCTTCTGT ACTTCTCCAA GCCCCCTCCT TTTTCCTAGG 900 CCTCACCTAC TCTCCCTCAT CAGTAAACCC TCCCAATAAC TCCAGCCCGG CTTCCTTGAC 960 TTCATTGCTT GCTTAAATCT AGTTTTACCA CCTATCTTGT GCCAGGAGCT CCTCTAAACA 1020 AATTGTTACT GACTTACACT TTTTGGCATA TCCTCCTCAG TGTCTGATTC AGGGCCAAGC 1080 TGGTAAGCTC TAGCAGCATG TGCTGAACTA AACGGACTGC CCTCTAAGGT TGGGCTCTGG 1140 ATAGGTAAAG ACAAAGAGCA CCCTGTGTCT ACTAAAAATA CAAAAAATTA 1190
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