Tag | Content |
---|
EnhancerAtlas ID | HS118-04408 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:47710220-47712020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr12:47710904-47710915 | TTTTATTGCTT | - | 6.32 | FOSL1 | MA0477.1 | chr12:47711732-47711743 | AGTGACTCATG | + | 6.14 | Foxd3 | MA0041.1 | chr12:47711066-47711078 | GTTTGTTTGTTT | + | 6.32 | LMX1B | MA0703.2 | chr12:47710227-47710238 | GATTTAATTAA | + | 6.02 | SPI1 | MA0080.4 | chr12:47711047-47711061 | AAAAAAAGGAAGTT | + | 6.11 | ZNF263 | MA0528.1 | chr12:47711150-47711171 | CTCACTGCCACCTCCTCCTCC | - | 6.11 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 47711000 | 47711452 | chr12 | 47710400 | 47711000 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I047316 | chr12 | 47710218 | 47711583 |
|
Enhancer Sequence | AAGCAGAGAT TTAATTAAAT ATTATGGCTT TTCAATAATT TTTGTTGTGT ACTATGCTCT 60 CCCCAAACCA GTAGCCTAAT AAAATTGAGT TTGAAAGTCC TCCATAAATT AACATGTTCT 120 AATAATTCTA TAAGAAAGAA TGGAGATACA ATATTTGATC TAGAAAGTGG ATATCCAATG 180 ATCATCTGAG CAAGGAACAC CATCCTCCTT AAAGTAAACA GCACACAGCT GTTTCCATCA 240 TGCTGACTGT AAGAAGATTA TCATACTCAG AAAAGAAATT CCAGGAAACT GCGTTCCAAT 300 TAACATGGAA ATGAATCCAC AAAATAAATA TGTATCCAGA GTTTATGCAA TCCCAGGGTA 360 CAATGGAGAC AGATGCAGAT TGATCTAATC TGGTTGCATT AGGAATAAGA ATGTTTGTTG 420 GGGAACATTG TGTGGAAAGT TGACATTTGG TTCAATCAGG AAGGCCAAAG TAGAAATTAT 480 GAAAGCAATT TCCTTTGTCC AGTTAAATTA GGCATTCAAA TAACAGGCTA CTCTTTGACC 540 TTCCTGGGAA AGGTCAGGAT GGCATCGAAT GGTCATTAAA TAAATAGCAG GCCTGTTCTT 600 GTAAATACTT TGTGAGACTT TAGGAAAACA TATTCTGGAT TGAAAATCAG CCAAAAAAGA 660 TCTGCAAGAA TTTCTCTAAC ATATTTTTAT TGCTTCTATT TATCCATTTT TAATTTGGAG 720 AAATAGTAAG TACTGGTAAA AGCACAAGAA CAAACTGAAT ATGGGGTCTA TTGAACAAAA 780 TTAAGAGGTC ACTTTTCTGC CACTTGCTAA TATGTGCTGC AGCTGCTAAA AAAAGGAAGT 840 TTTGTTGTTT GTTTGTTTTG GTTTTGGTTT TGGTTTTGAG ACGGAGTTTC GCTCTTTTGC 900 CCAGGCTGGA GTGCAATGGC GTGATCTCGC CTCACTGCCA CCTCCTCCTC CCGGGTTCAA 960 TTGATTCTCC TGCCTCAGCC TCCCAAGTGG CTGGGATTAT TGGCAGGTGC CACCATGCCT 1020 GGCTAATTTT TGTATTTTTA GTACAGACGG GGTTTCACCA CGTTGGCCAG GCTGGTCTTG 1080 AACTCCTGTC CTCAGGTGAC CTGCCCGCCT TGGCCTCCCG AAGTGCTGGG ATTACAGGCG 1140 TGAGCCACCG CACCCAGCCA GAAAGAAGGT TTTTTGAAAA ATAGCTCCTG TGGATGTCTC 1200 CCCAAGGCTC CACTTGATAT AGCTAAGGAG AATTCCTGGC ATGTATCATA AGATATATGG 1260 TTTCTTAATT AGATGGGTGA CTTGCAGGAC TAGAATTTAA GAACACTCTT CATGCTGCCT 1320 TAGGTTATAA TTCCCAGCTT GCATTACAGC AATGGACATG CTGTTAATAT TTTCTCCAAC 1380 AGTCCAAACT GCAAGTATAT GAAGTTAAAT CAAATCTCTT TTCTTGTCCA TTAAAGTTCA 1440 AGTTGCCATA ATAAAAGCTG GCAAGTTGTT TTTATAAACA CTAAATTAAT AGAACAGATT 1500 TTGGCTGGGC ACAGTGACTC ATGCCTGTAA TCCCAGCACT TTGGGAGGCT GATACAGGAG 1560 GATCACTCAA GTTCAGGAGT TCAAGACCAG CCTGGGCATC ACAGGGAGAC CTCGTCTCTA 1620 TTAAAAATAA AAATAAAGAC AACTAGCCTG GCTTGGTGGT GTGTGCCTGT GGTCCCAGCT 1680 ACTTGGGAGG CTGAGGTGGG AGGATCCCTT GAGCCCAGGA GTTGCAGTGA GCTATGATTG 1740 CACCACTGCA CTCCAGCCTG GGTAACAGAG CAAGACCTTG TCTCAGAAAA CAAAACAAAA 1800
|