Tag | Content |
---|
EnhancerAtlas ID | HS045-71405 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr9:136543870-136545670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PPARG | MA0066.1 | chr9:136544588-136544608 | ACTTGATCACCGTGCCCCAC | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 136545200 | 136545422 | chr9 | 136545444 | 136545523 |
| | Number: 1 | ID | Chromosome | Start | End |
GH09I133679 | chr9 | 136544278 | 136545419 |
| Enhancer Sequence | AAGCATAGGA ACCGTCTTCC CTGGGTCTCT GGGTCCCCCT TTCTGATGGC TCCCATGTCA 60 CATAAAGCTC TGATTAAATC TATCTGGTGT GCTTTTCTCT TGTGAACCAG TCTTTTGTTA 120 CAGGGCTGTC TCCCATGCCC CTGATAATGG GTGAGGGGAG GGCTCACACC TTTTCTTTCC 180 TTACAAGGGC AAGATGAGAA CCTGGAACCG ATTGCCCCTG AAGTCTCCAA GGCCCCCAGC 240 TCAGAGCCCT CTGCACCCAG TTCTGCCTGA GGTCACTTGC CCCAGACAGA AGCAGCAAAC 300 CCGGGTGGGG GTCGAAGCTT CCCACCACCC ACTCCACAAA CACCCTCGCT CCAACTTCCC 360 CTTGGGGCCC AGGCCCTTCA CACTATCGTG GCAACAGCTC GACCCGTGAC AGGGAACACG 420 GTGCCCCAGC CTGCGGCCAC CAGTCTCTCT GTGCTGCATC AGGGAACCTG CCCATGATAT 480 CGGGTATCTG TCTCAGGCCT CAGCAAATCT GCACGGGTTC TGTAAAGCGA GTGTTTAGGC 540 AGTGGCTGGA ACTCAGCTGG TCTCTGACTG GCATGTCATA GTTATCTAAC GTGTGTGGGT 600 GCAGGACTGC TCCATCCTGA GCTAATCAAA TCCTAACAGC GCCGCGACTA GGACTTCTCG 660 CTGTCAGGAA AAGAGATTCA ATTTCCTTTT GAGCTGAAAT TAATTTTCAG AGAAAATCAC 720 TTGATCACCG TGCCCCACGG AGTGCTCCCA GCCCAGCATG CTGCTTCGCG GCGGGGCCCG 780 TCCTCGGCAG GGGCCCTGGG AACACCGTGT CTGGCCGAGC GGAGCTCTGG GAGACACGCC 840 GGGAGAGCAC TGACCCACGG GGAATCTTGC TGGCCTCGAG GCAAGATATT TGGGGAGCAA 900 GGACAGCTGG TCTGCTGGCT GCTGAGCGGA CAATAACTTC TCCCCACCCT GCTTCCTCCT 960 CTAGCAGTCC AGGGATCGTG GCAGCCTGGG TCAGATCCCA GCCTCTCGGA GAACAATCAC 1020 TGCACAACAG CAGCAGTGCT CAGCTGGGAA TCGCGCCCAA TTCGTCTGGT GGTGAGGAGG 1080 GTCTTTGGGC AGCGGCAGGC GCCCGCTCTC GCACCCGGGG CCCGGGTCTG CAGCTCTGGC 1140 CCTTGTCCTC ATCGGCCCTC ACAACTGCTT TCAACCCAGA GGTTCCGCTG ACTGCGCAGG 1200 CACACGCATT CCTCGCCTGC ATCTGGTTGG CTGGAACCCA ACTGATCGCC TATAAATACC 1260 TGGCTCAGGC CCACGCTCCA GCCCAGCGTT TCTTCACGTT GAGGGATATG TCATCAACAC 1320 ATTTTTAAGC CAGCACAAGA TATTATTTAG GAGAATATGA AATTCTCCCT GGATTCAGAG 1380 AATCCAGAGT GTCTGGACAG ACTTATGGAA AGGCCCGGAA AGAATTTTAG ACATTGTGCT 1440 AGACTCCGTG CTACAGGTGG GGACACTGAG GCCCAGAGAG GCGACCCGCA GAAGGACCGG 1500 GCAGGATGGG AAGCCAGGCT TCTGGCCTGA GCTCCACCGA GCCTTGGGTA ACATGGATGC 1560 TTTGGTCCCA AACCCCCCAG TGTCTGTGGC TGACTCAACT CCCATCTCCC ACCTGCCTGT 1620 GAGGCCCCCT ACAGGGGGAG CTGGCCGTGG CCAGTGGCTG TATCCCCACC CGTCTTGCTG 1680 GCCAGGAAAT GGGGAGGGCA CTGTGTCCCA GGCTGGGGCC ACCTGGGAGC GCGTGGCCCT 1740 GGCCACTTTG AGGGACAGCC TCCCAGGTCA GCAAAAACTG TAACATTGAC ACTAAGGGCC 1800
|
| |
|
|
|