Tag | Content |
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EnhancerAtlas ID | HS012-18794 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:185089880-185091080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXC11 | MA0651.1 | chr3:185090068-185090079 | ATTTTACGACT | - | 6.02 | Mecom | MA0029.1 | chr3:185090603-185090617 | ATGATAAGATAACC | + | 6.36 | SOX10 | MA0442.2 | chr3:185090542-185090553 | AAAACAAAGAA | + | 6.62 | ZNF263 | MA0528.1 | chr3:185090095-185090116 | TCCCCTTCCTCCTCCTTTTTC | - | 6 | ZNF263 | MA0528.1 | chr3:185090092-185090113 | CCTTCCCCTTCCTCCTCCTTT | - | 7.99 | ZNF263 | MA0528.1 | chr3:185090089-185090110 | CTCCCTTCCCCTTCCTCCTCC | - | 9.25 |
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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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Enhancer Sequence | TCCCATAACA AATTTAGATA CTATGCACAC TAAGAAGGAA CAGATGCAAC ATACCTTTGG 60 ATATTTCCAG CCACTGCTTC CAGACCTAAA TTACAGACCC ACTTTCATTT TTGCTAAGCA 120 TAGAAACTGC TGGGAAATAC TCACCTGATG TTACAGCCAT TAGGGCTCAA GAGCCCATTT 180 ACAAAGACAT TTTACGACTT TGCCAGGTTC TCCCTTCCCC TTCCTCCTCC TTTTTCTGGC 240 CATTTTGGAG TAGGATTCCT TCCATCTGTT TGTCTAAGAA AAAATAATAG ATCATTTGCT 300 TGTGTTAATG ATTGAAGCTA TGCCCCAATC TAGTCTTTTA AGTATTCTCA AAGACCTAGA 360 GACAGACTAG ACCAGGTTTC TTGGAGAAAG AAAAACAGTC ACATAATCTT TTATATTTTC 420 TGTAATAATT TCTTTTCTCC AATCAGGGCT TCCACCATAA CACATTGAAA AGTACTCACT 480 CATCATCTGC TCTCCTTTGA TTAAAAGGTT ATCTACATTG ATGATAAGGA TTTCTTTTAA 540 CTGAATCTTA GACCTTTGAT ACCAGATTTT GTTAAAGCCA ATCTGCTTTT GTCACAAATT 600 TTCTTATAAA CAGCCCTTAT CTTTTTTCTG CTAACTATTT AATAGGCTAT GGAATGGCTT 660 TAAAAACAAA GAAGAGCCAA CCAGTTCTAA TAGACTTTGA CCATATCTGA AACGTAAAGA 720 GAGATGATAA GATAACCTTA TTATTAATGC AGAGCAAAGA GGACCCTAAG ATAAGGTTCC 780 TCTTTTTCCC CTGCCAGGAA AAGGAAGTCA CTCCAAGGGA ATACCTGTAC CTGAGACTGT 840 CCTGCTAAAG CTTCACCAAG CTCATGAGAA ATATGAAATG ATCATTTTGA TCTACCTGAA 900 ATACATAGAA CTTGTACCCA GAAATTCTTT ACATTGACAA ATAGTTATGG ACTTGAATTG 960 GCTGTGTGCT GGACTTGAAG TTTTGGGGTA AGGAAATGAT AGTCTTGAGA GTTCCATGTT 1020 CTAAGAAATC ACTTCTGGTT TATTCTTGGG TAGTGATAGC CAAGGATTTG TCAGAGACTG 1080 GGAAGCTAAG CTTCTGGGCC TTGTTTTGGA CCTGTGCTTT CATAGCTGTA TATTATTTTT 1140 CATCACAGGA AACTGAAAAA GTAGAAACAA ACGAACAAAA ATGTATCTTT GATACTTTTT 1200
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