| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01228 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:33182050-33183240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr1:33182323-33182338 | GTGGAGGGCGTGGCC | - | 6.36 | | ZEB1 | MA0103.3 | chr1:33182942-33182953 | CGCACCTGCCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23116 | chr1:33181123-33183255 | Colon_Crypt_1 | | SE_26629 | chr1:33181022-33183324 | Esophagus | | SE_41588 | chr1:33181113-33183198 | LNCaP | | SE_65538 | chr1:33180964-33183410 | Pancreatic_islets |
|
| | 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 |
| GH01I032715 | chr1 | 33181165 | 33183189 |
|
Enhancer Sequence | GGACTGCAAG AAGGTGGGAG TGCCTGTCAG GGAGCTGAGG AGCAGTGGGG AGGCGTAGGT 60
TGCCAAGCAG CTAACCAGGG CAGGCAAGAG GTGGGTCTGG AACCCAGGCT TCCCCATTCC 120
CAGCAGGAGC ATCCCCTGCC TACTCCCCAC CCAGCTCTTG GCACTGGAGT CCTGGGTTCA 180
AGTCCCATTC TCCATTTGAC CCCATCTGAA AAACATGGGC ACAGACCCTG TGAGGTCAAC 240
ACCTGGGATT CCTGCTCCTT TAAGCCTTTC CCAGTGGAGG GCGTGGCCCT GGCTGCAGGT 300
GAGCGCTGTT GCCACATCAG CCGGGTAAGC CCTGCCCTGT CCCCTCCCCC AGCTCTGGAG 360
AGAGGCCCTA GAGGCCCCAG AGGACGGTGG GAAGTGGGCG GGGAGAAAAG GCGGAGCCTG 420
CTTGGCTGGA GAGAAGGGGA CAGCCCTGGG CTGGGTGAAG GCACCTGAGT GTTGAGAACA 480
CCTGACTGTG CTAGCCTCTG TGTGTCTGTG AGGGTGTCTC TGAATGTTCC AGAGTGCACA 540
GGAGTGTGTA CAAAATAAAC GTGCACTTTG ACTGTGAGGA TACAAGGTTG TATGCAAGAC 600
TGCCTGAATG TCTCAAATAC CTCTTTTGTG TGCCTTTGTT TCTGTGTGGC TGTCCCTGGG 660
TGTGCAGGAG TAAGTATGAA TGTGTTTGTT TGTCTCCAGC GTGCCTTTGT GTGGCCAAGT 720
GTGTGTGTGA CCCTCTGAAT AAGTCTCAGA ATAAACCTGA GCTTTTGTGA GTCCACATTT 780
AGAAGTGCCC CTCCAACTGG CCCCAGGCTG ATGGAGGCAT AAAGCCTGCC CCATCCTTTA 840
GAAAAGCCCA GCCCCTGTGC CCCCTCTCCC TTCCTGGTGA CTCACTGCCC CCCGCACCTG 900
CCCCCAACCT CCAGAGCCTC CTGCCTTAAA GAGCAGTCCC TCTCTTGCCC AGCTTGTCCT 960
CTCAACACTC AAAGGAAGGC TCAGTCCCCT CCTCTAGGTG GACTTCTGTG ACCAGGGAAG 1020
GGGGGCCTTA CATTATTTGC TAAGCATCTT CTATTGTACC CCCATTTGAC AGATGACGAC 1080
ACACAGCCCA AAGCAGTGCA GTGACCTGCT GCAGGTGGGC ACTTGTGTTT GATTCCATGA 1140
CTTTTTTTTT TTTTTTTTGA GACAGGGTCA TGCTCTGTCA CCTAGGCTGG 1190
|
