Tag | Content |
---|
EnhancerAtlas ID | HS047-08802 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:122116700-122118030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr12:122117424-122117435 | TCTTGTTTACA | + | 6.02 | Myod1 | MA0499.1 | chr12:122116754-122116767 | AGCAGCTGCCCCT | + | 6.18 | NFYB | MA0502.1 | chr12:122116834-122116849 | CTGATTGGCCCAGCT | - | 6.42 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_49991 | chr12:122116258-122117608 | RPMI-8402 |
|
| 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 |
GH12I121678 | chr12 | 122116259 | 122117608 |
|
Enhancer Sequence | CCCCTCCCCG CCTCAGTCTT TCTGGTTCTG TGAATCAGCT TTCTCATGGT GGGAAGCAGC 60 TGCCCCTTTT ATCACCTCAG TTCCAATCCC TCAAACAAAC TTACTGGCTG TTTCTGAATT 120 CCAATCCCCA AACCCTGATT GGCCCAGCTG GGTCTGGAGT CGGCCCCTGG CCAGTCATGC 180 TGCTGCCACT GTGGTTCTTT TTATGAAATT TTCCTCTCCT CCTTAGGTAC CTAGCCAGCA 240 GCCCAGGCCC ATCTTCAACC CGGTACAAAC TGTCTCTTGC CTGTTGGCCT GTCCAGAGCC 300 ACCCTGCCAC TCGTTGAGGG GTGCCTCATG ACTTGGAACC TTCTCTTCCT TGACCAGCCT 360 AAGACACAGC CCCAAGCCTC AGTCCCAGCA TGGCAAAGAG CTCATTCGCA GCCCCTAATC 420 AGACCCTGGC TCAGAGGAAG CCAGGACCGC CCCATCGAGA AGAATCTGGG CCAAATTAGG 480 GCTCATCTGC ATCTGCAGGC CAGCCGGAAG GGCAGGTTAC ACAAATCTAT GAGATTATTC 540 TCCCTATGGG GTCAGAGTTG GGTAACATTA TTCACAACAC CTGAGTAGGT GGTTCAGGCT 600 GGCCCCTCCC AGATACTGAC ATGCCAAGAG CATTAGGCCT GGGGGGCTCC TGTCCCAAAT 660 ACCCTTCGGG TAATCACTTC CAGATCTGAG TGGCAAGGAT ATGGCTGAGC GCCATATTCA 720 AGGATCTTGT TTACAGCTTT GGGTGAGAGG AGTTGCCCTG TATAGTCTGG GGCAAGAGGG 780 ACTCCCCTCA ACACCCACAG ATAAATGTCC CCTCAATCAG CAAGGCATGG TCTTGTTGAC 840 CCTCTTCTGG GCACAGACCT TTAGCTTTCT TCCTGGATGT TCAGCCTTGG CAGGGAGTCC 900 TGAGATTTGT TTTTTTTTTT TTTTCTTTTA CAGAGTCTCG CTCTGTCACC CAGGCTGGAG 960 TGCAGTGATG CGATCTTGGC TCACTGCAAC CTCCACCTCC TGGGTTAAAG TGATTCTTGT 1020 ACCTCGGCCT CTCAAGTAGC TGGGACTACG GGCACTGCCA CCATGCCCGG CTAATTTTGT 1080 ATTTTTAGTA GAGACGGTTT CACCACGTTG GCCAGCCCGG TCTCCAACTC CTGACCTCAA 1140 GTGATCCGCC CACCTCGGTC TCCCAAAGTG CTGGGATTAC AGGCATGGGC CATAGCACAT 1200 AATAGACAAA AGGTGGACAC CATCCAGATA TCCATCAATA GATGAGCAGA TAAACAGAAT 1260 GCGCTCTGTT CATGCCATGG AATCCTATTT GGCTATAAAA AGGAATGAAG TTCTTTTTTT 1320 TTTTTTTTTT 1330
|