Tag | Content |
---|
EnhancerAtlas ID | HS142-00366 |
Organism | Homo sapiens |
Tissue/cell | NCCIT |
Coordinate | chr1:33181780-33183110 |
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: 2 | Chromosome | Start | End |
chr1 | 33182280 | 33182513 | chr1 | 33182034 | 33182786 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I032715 | chr1 | 33181165 | 33183189 |
|
Enhancer Sequence | CTGTATTATG TAGTTAAATT GTCTCATCAA TCCTGTGAGG TGGGTGTGAT CACGCCTCAT 60 TTACAGATGA GGAAACTGAG GGTCAGAGAA CAGCAGTGAC TTGCCCTAAG TCACAGAGCT 120 GGGAAAGAGC TGGCTGGTTG CCTACTGCAT CTTCTACCCA GGTTCAGGAA ATGTTTAGGG 180 ATAGATTCCA CAGGTAGAGA GAGGTGTGTG GCGGGATGCC CAGGTTTCTG GCTTGGGTGG 240 CTTTCAGGAG AGTGCTGACT CCTGAGACAG GGACTGCAAG AAGGTGGGAG TGCCTGTCAG 300 GGAGCTGAGG AGCAGTGGGG AGGCGTAGGT TGCCAAGCAG CTAACCAGGG CAGGCAAGAG 360 GTGGGTCTGG AACCCAGGCT TCCCCATTCC CAGCAGGAGC ATCCCCTGCC TACTCCCCAC 420 CCAGCTCTTG GCACTGGAGT CCTGGGTTCA AGTCCCATTC TCCATTTGAC CCCATCTGAA 480 AAACATGGGC ACAGACCCTG TGAGGTCAAC ACCTGGGATT CCTGCTCCTT TAAGCCTTTC 540 CCAGTGGAGG GCGTGGCCCT GGCTGCAGGT GAGCGCTGTT GCCACATCAG CCGGGTAAGC 600 CCTGCCCTGT CCCCTCCCCC AGCTCTGGAG AGAGGCCCTA GAGGCCCCAG AGGACGGTGG 660 GAAGTGGGCG GGGAGAAAAG GCGGAGCCTG CTTGGCTGGA GAGAAGGGGA CAGCCCTGGG 720 CTGGGTGAAG GCACCTGAGT GTTGAGAACA CCTGACTGTG CTAGCCTCTG TGTGTCTGTG 780 AGGGTGTCTC TGAATGTTCC AGAGTGCACA GGAGTGTGTA CAAAATAAAC GTGCACTTTG 840 ACTGTGAGGA TACAAGGTTG TATGCAAGAC TGCCTGAATG TCTCAAATAC CTCTTTTGTG 900 TGCCTTTGTT TCTGTGTGGC TGTCCCTGGG TGTGCAGGAG TAAGTATGAA TGTGTTTGTT 960 TGTCTCCAGC GTGCCTTTGT GTGGCCAAGT GTGTGTGTGA CCCTCTGAAT AAGTCTCAGA 1020 ATAAACCTGA GCTTTTGTGA GTCCACATTT AGAAGTGCCC CTCCAACTGG CCCCAGGCTG 1080 ATGGAGGCAT AAAGCCTGCC CCATCCTTTA GAAAAGCCCA GCCCCTGTGC CCCCTCTCCC 1140 TTCCTGGTGA CTCACTGCCC CCCGCACCTG CCCCCAACCT CCAGAGCCTC CTGCCTTAAA 1200 GAGCAGTCCC TCTCTTGCCC AGCTTGTCCT CTCAACACTC AAAGGAAGGC TCAGTCCCCT 1260 CCTCTAGGTG GACTTCTGTG ACCAGGGAAG GGGGGCCTTA CATTATTTGC TAAGCATCTT 1320 CTATTGTACC 1330
|