Tag | Content |
---|
EnhancerAtlas ID | HS101-03082 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:167012720-167014230 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I167043 | chr1 | 167012838 | 167014050 |
|
Enhancer Sequence | TCATGGTATG AATTGTACTT AAGCAACTAA CATCTTTATT TAAGGGTTCT CTCAATCTCT 60 TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC TAACATAGTT AGACCTGAGT 120 TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC TTTAATATCC 180 CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA TAATGTGGCT 240 GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT TCTTCTTTCA 300 TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG ACAACCTCTA 360 GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG AGATTCACTG 420 AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT GAAGCCTCTT 480 CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC TGCTCCAAGA 540 CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC ACAATAAGCC 600 CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT TGATTGCCAA 660 GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT ACAGAAATCC 720 ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC CTTCGGCCAC 780 AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT 840 GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA GACTGACAGG 900 GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA GAAAAGCTTC 960 TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA AAAAATCATA 1020 GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT TTCAACTGTG CAATTCCTCT 1080 TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT GGGCTTGTTT AAAATACTTC 1140 AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC CTCTTTCGGG CTTTCCTTTC 1200 CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA TCTGTGATAA AGCTGTCCAC 1260 AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC TCAGGGCATG TCCTCCATGT 1320 CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA TCAGCCAAAA CTCTCCCTCC 1380 CCAACCCCAA CTCCAGGCGC TTATACCTCA CTCCCCACAG CTGTTTTTAT TATTCGTATT 1440 CACTGCTACT CAATCCCATC TTGTTTTCAA GAGGACTTAA GGTGGATTCC ACAAATACAT 1500 AAAAGATGAG 1510
|