| Tag | Content |
|---|
EnhancerAtlas ID | HS086-00452 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:33181880-33183090 |
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 | TTGCCCTAAG TCACAGAGCT GGGAAAGAGC TGGCTGGTTG CCTACTGCAT CTTCTACCCA 60
GGTTCAGGAA ATGTTTAGGG ATAGATTCCA CAGGTAGAGA GAGGTGTGTG GCGGGATGCC 120
CAGGTTTCTG GCTTGGGTGG CTTTCAGGAG AGTGCTGACT CCTGAGACAG GGACTGCAAG 180
AAGGTGGGAG TGCCTGTCAG GGAGCTGAGG AGCAGTGGGG AGGCGTAGGT TGCCAAGCAG 240
CTAACCAGGG CAGGCAAGAG GTGGGTCTGG AACCCAGGCT TCCCCATTCC CAGCAGGAGC 300
ATCCCCTGCC TACTCCCCAC CCAGCTCTTG GCACTGGAGT CCTGGGTTCA AGTCCCATTC 360
TCCATTTGAC CCCATCTGAA AAACATGGGC ACAGACCCTG TGAGGTCAAC ACCTGGGATT 420
CCTGCTCCTT TAAGCCTTTC CCAGTGGAGG GCGTGGCCCT GGCTGCAGGT GAGCGCTGTT 480
GCCACATCAG CCGGGTAAGC CCTGCCCTGT CCCCTCCCCC AGCTCTGGAG AGAGGCCCTA 540
GAGGCCCCAG AGGACGGTGG GAAGTGGGCG GGGAGAAAAG GCGGAGCCTG CTTGGCTGGA 600
GAGAAGGGGA CAGCCCTGGG CTGGGTGAAG GCACCTGAGT GTTGAGAACA CCTGACTGTG 660
CTAGCCTCTG TGTGTCTGTG AGGGTGTCTC TGAATGTTCC AGAGTGCACA GGAGTGTGTA 720
CAAAATAAAC GTGCACTTTG ACTGTGAGGA TACAAGGTTG TATGCAAGAC TGCCTGAATG 780
TCTCAAATAC CTCTTTTGTG TGCCTTTGTT TCTGTGTGGC TGTCCCTGGG TGTGCAGGAG 840
TAAGTATGAA TGTGTTTGTT TGTCTCCAGC GTGCCTTTGT GTGGCCAAGT GTGTGTGTGA 900
CCCTCTGAAT AAGTCTCAGA ATAAACCTGA GCTTTTGTGA GTCCACATTT AGAAGTGCCC 960
CTCCAACTGG CCCCAGGCTG ATGGAGGCAT AAAGCCTGCC CCATCCTTTA GAAAAGCCCA 1020
GCCCCTGTGC CCCCTCTCCC TTCCTGGTGA CTCACTGCCC CCCGCACCTG CCCCCAACCT 1080
CCAGAGCCTC CTGCCTTAAA GAGCAGTCCC TCTCTTGCCC AGCTTGTCCT CTCAACACTC 1140
AAAGGAAGGC TCAGTCCCCT CCTCTAGGTG GACTTCTGTG ACCAGGGAAG GGGGGCCTTA 1200
CATTATTTGC 1210
|
