| Tag | Content |
|---|
EnhancerAtlas ID | HS101-17274 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr16:70256400-70258260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:70256442-70256454 | AAACAAACAAAC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTAGCTTGT ATTCCTACGC AGCCTGTGGA ACCATTAAAA AAAAACAAAC AAACAAAAAC 60
AGAACAAATC CTAGGAAGAC AGCAAAGTAC ACAGCATTTT TCTGACAAAA TTCCTTCCAC 120
GAGGATGTCA TTATTTTGGT TTTTATGTTG AAGATGTGAC TACCACTTAA TTAGTACTCA 180
AATTGGAGTG GCAAACCAGA AAGTCACAGC TACAGACTTT CAGTAGAGCT GACTCGCCCC 240
TGTGTCTCCT TCCTGTTTTC ATGTGTTGCA GCCTGTTCTC TTCAGAGCCT AACACACTGA 300
CAGTAGACCT CTGCAGGACA ACTTTGACAC CCAGTTCTCT CCAAGCTGCC AGTGAGCTCC 360
TTGTGCAGCC TCACTCCTCA CCTACAGCAT GAGCCCTTGC AGCTCTCCCA GCATCATAAT 420
CTTGTATCTC AGTCCTGGCT TCTTTCACTG CTGGCATCCC TCCATCTCTC CCTTTTTCAC 480
CTACTTTTCT TTTTTCAAAG AATTCTTCTC TTTCATCTGC TTTTATGAAA AATAATGACA 540
CCTCTGAAAT TCTTTCCTGT AGTCCTGCAG CATCAATGCC AGGAAGACAG GCCTCATCCT 600
CCCAGCTTCT ATGCTGCTCC TTTCAGATCC CTTACCCTGT CCCCATTTTC ATGACACGGG 660
CTCTCCAGCC AGGAAGAAGA CACTGTTTCT CACTCTCTCT CTTTTCCATC TTTGCCTGTC 720
CCTCTCGCTG TGTAACTTCC CTTATAACTC AGCCTGAGGC CAGTGCTAGA AAGGCACATC 780
ACCTGACTTA TTCTGTGCCT GATTCTACCT AGATCAGTGC AACCACTGGC TTCTCAGGGG 840
GACCCTTGAG TACTGGGCAC TGATGAACTG CTGCCAACAC ATTCGTCATT TCTGCCATTA 900
AAAGGTCCTA AGTCCTCTCC AGTGACAGGT TCCTCAAGTC CCCACTATGC TCTATAATGC 960
CCTATGCTTT CAGCTAATGA CTCAGTCCTC AGAAAAACAA ACAAATAAAA AAACACAGGC 1020
TTTAATTTCC TCTACCCCTA CCCCCAATCC ACCATACACT GCCAAAATTC TGTCTATACC 1080
AACTTTGACT GCTTTCCTTG AGGCAGAGAA AAGGTGAGGG CCAGTTAATC TATCAATGTT 1140
CTTTCTCCTG TTTCTTCAAC CTCTGCTTTC TAGTGGCTCC TTCCCCTTGG CCAAAAGAAC 1200
ATAATCTCTC CAACATTTAA AATAAACATC TCATATCTCC CTCCAGCAAT AGCTTCCTAT 1260
CCTCGACTTC AAGAAAAACT CACTGACCAA ATAACTTACC TCAAGCTTTT CATTTTCAAA 1320
TGTCTCTACC ACTCAATAGT ATTCAATCTA GCTTCTTCTG TCTCTCTACA AAACTCTTTT 1380
TCCTTATAAT CCCTAGAGCA TCTGACAAGG CTGACTACTC CCATCTGGAT GTCCTATATC 1440
TAGGACACTT CCCTTCTCAA TGTCCCTGTA TTTTTTTGAA TGGCTTCCTC TTCTATACTT 1500
TCACAAAAAT GCTAAACTAG GATTCTGACC CAGGCCTTCC TTCCTCTTCA CTCACTATTC 1560
TCCAGAGGCT TCTCTCTGGT TTGGTTGCTT ACAAAGGCTC TAGAGTATAG AGACTGAAAA 1620
GGAAACAGGG CCTTTTCTGT GTACTAATGA TGTGCAAATC TCTCAAGCTT AGACTTTCTC 1680
CTTAGTTCAA AATCCAATTT TTTTTTTTTA ATTGATCATT CTTGGGTGTT TCTCGCAGAG 1740
GGGGATTTGG CAGGGTCATA GGACAATAGT GGAGGGAAGG TCAGCAGATA AACAAGTGAA 1800
CAAAGGTCTC TGGTTTTCCT AGGCAGAGTG TGTGTGTCCC TGGGTACTTG AGATTAGGGA 1860
|
| |
|
|
|
