| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18768 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr3:183182070-183183050 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr3:183182611-183182623 | GTCTGTTTACAT | - | 6.44 | | FOXP2 | MA0593.1 | chr3:183182612-183182623 | TCTGTTTACAT | - | 6.02 | | Foxo1 | MA0480.1 | chr3:183182870-183182881 | TCTTGTTTACA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGCCTCCCG AGTAGCTAGG ACTACAGGTG CATGCCACCA TGCCCAACTA ATTTTTGTAT 60
TATATTAGTA AAGACGGGGT TTCACTATGT TGGCCAGGCT TGTCTCAAAC TCCTGACCTC 120
GTGATCCACC TGCCTTAGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCGCGCCC 180
GGCTCTCTCC ACACTCTTCT TAGATGTCCC ATCTGCTCCT CCAAGCATCA GACCAGTGTT 240
CCCCAGGTGT GTTCAGTCAG ATGACCTGTT GGCACCTCAA CATGTTCAAA GCTGAACTTA 300
CCATCTTGCC ACATTGCTAC TAACCTCATT ACCTTGAACC TCTTCCCTAA TCTAGACTTC 360
AGCAAACATA TCCAACTTTT CCTACCTTTG GTCTTGTTTT ATCTAATCCA TTTACTGTGC 420
AGCCCCCAGG GTACAGAAAC AGCTGGATTG TTACATCATA GTGTTTGCCT TATTTGAACA 480
CAGTTCGAAC AGTTGGCCAC CTTTGGCCGA AACTCAGTGA TTGGTACAAG ACTAGATTAC 540
AGTCTGTTTA CATATCCAGT TAGGTGACAC TTCACTATGT ATGGAGAAAC CTTTAGGCTG 600
AACTTAAAAT ATGTAAGGAG GCAGCTTTAG CCTAAACTTA ATTTAACAGG TGGTAGCAAA 660
GGTTCTAAGG AGGGAGATTC TTCATTCAAC AAGCAGGGAA CCCTACCCGA GAGGGGCAAC 720
ATGAAGGCAC GCAGGCTTGG GCTCACTCCT GTTTCCCAGC TCATCCTTGT AATAAATGTT 780
TTTCACCATC AGGACATACT TCTTGTTTAC ATATGACCTT TAGCAGAATA CGTATACATG 840
ATATAAAACA GGATGATTGC CAAGTAGCAA TTTTAACTGC TACAATACAC TTTATCAGCT 900
CTCATATATC TACCTGTTTG AAAATGCTTA TCTGGGCCAA GCGCAGTGGC TCACACCTGT 960
AATCCCAACA CTTTGGGAAG 980
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