| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09373 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:10305580-10307050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:10306717-10306729 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:10306721-10306733 | AAACAAACAAAC | - | 6.32 |
|
| | 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 |
| GH12I010152 | chr12 | 10305421 | 10307199 |
|
Enhancer Sequence | AAATAAATAA ATAAAAGTCT TTTATCTTTC AGCTCTTGGA TCATTTTACT GGATTCCTTG 60
GATTGCGTTT CAACAGCCTC CTGAGTCTCA GTGAGCTTTC TTTCCATCTA GGTTCTCATT 120
TCTGTGTCTG TCATTTCATT CTGGTTAAGA GCCATTGCTG GGGAGCTAGT GTGCTCATTT 180
GGAGGTAAGG GGACACTCTT ACTTTTTAAT TGGCAAAATT CTTTCTCTTC TGAGAGGGCT 240
GGTATTCCTT TAACTGTGGT GTAAGTTGAA TATAGTCATT TGCTTCATTT ATGAGTGCTG 300
TCAGAGGGCC AAGGCTCTGT ACAAGATCTT TGTGGCTGGA TTCTTGCCCT GAGTTTCACA 360
GACCAATATT TAATATATTG GCAGAATATT TTTGGTGTAA TTTGGGCTAT CATCCAGCAG 420
ATGGCGCATA AGAGTAACGG CCAGCGCTGC GGGTTTTTAC GTTTCAGCGA GCTCGCAACA 480
ACGTCCTGTG GTGTGGCCCA GCGCGGGGAG CTGACCCCAC CAGCTCCGCT CTCAAGCCTT 540
CGGAGAGTCC TCTCCAGTCA CTATCGTCAT TCCCGCATTT CCTTTGCTAG GCTGTCCGGG 600
CTGGGCAGCT CCCTCAGGCG GACACCCATG GCTGGCAGAC CTTCCGCGCC TGCCCCTAAT 660
CTGGGCATAT CACTCCCTCG GTTTTCTGAG ACTCGGGACT CCTTGCCCGC TGGAGCGCAG 720
GCCATGAATC TGGGTCCCGC ACTGCGGCGC TGCACGCCGC AGCCCAGGGC TTTGGCCCCA 780
GCCAGCACAT CCGCCATCCT GCACCCCAGG TTCCGGCACG GGCTGCGACG GGGCCTCGGA 840
ACTGCTCCCA AGCGGCTGGG AAAGAACTCA GTCAGGCATG TCGGCCTGCA AAGCACCCAG 900
GATGGGCAGT GGAGTCTGCA CCGTTGACAG GCTCCTAGAG CGGCCAGGCA GAGGACTTGA 960
GAGGGGCTGG AGGGCAGGAG GTCCTGCGGA ACAGAAGTGC CCCACTCCGA AGGGAAAGTC 1020
GACCCTGCTG TTCTCTTTGC GCGGCAGTCA GTGGGGTTAG AGTTATTCGG AAGAGGACGG 1080
AGAGCCTTGG GGGATGGGTG CGCATGGCCA TGTTCCACTG GAACTGCCCC CAACGCAAAA 1140
CAAACAAACA AACAACAACA ACAACAAAAA CCGGGCTCTA TGCAGGCTGG AGTTCTGCCT 1200
CTGCCTGCTT GTAGGGCATA TCCCCATGCC AGTTCGAATG TTTATGGGGA GTGTAGGATC 1260
TCTTGTGGCT GGAATCCTAG AGGTCCACAG CAAGAGTGGG CTGCCTTGCC AAGGGTTGTT 1320
CAGGGCCAGG AACTGGCACT GGTGTTCCAG AACCTGAAAG GGTTCCCGGT CTCCCTTTCT 1380
GTCAGCGGGA GTGGTGCTTC CTGTCTGCGT CTATTTGGCC ATCTTGTCTC TGTTGACCAA 1440
ATAGCTTTTT TGAGAAGAAA AATGAAATTG 1470
|
