| Tag | Content |
|---|
EnhancerAtlas ID | HS089-00009 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr1:999820-1001620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr1:1001171-1001181 | GTCACGTGAT | - | 6.02 | | MITF | MA0620.2 | chr1:1001167-1001185 | GCAAGTCACGTGATCACA | + | 6.31 | | MITF | MA0620.2 | chr1:1001167-1001185 | GCAAGTCACGTGATCACA | - | 6.31 | | PLAG1 | MA0163.1 | chr1:1000247-1000261 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000277-1000291 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000307-1000321 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000337-1000351 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000367-1000381 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000397-1000411 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000427-1000441 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000457-1000471 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000487-1000501 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000517-1000531 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000547-1000561 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000604-1000618 | GGGGCCCTGGGGGG | + | 7.03 | | PLAG1 | MA0163.1 | chr1:1000664-1000678 | GGGGCCCTGGGGGG | + | 7.03 | | RREB1 | MA0073.1 | chr1:1000579-1000599 | CTGGGGGTGTTGTGGTGGGG | - | 6.08 | | RREB1 | MA0073.1 | chr1:1000639-1000659 | CCTCGGGGGGTGTGGTGGGG | - | 6.41 | | RREB1 | MA0073.1 | chr1:1000282-1000302 | CCTGGGGGGGTGTGGTGTGG | - | 6.6 | | RREB1 | MA0073.1 | chr1:1000402-1000422 | CCTGGGGGGGTGTGGTGTGG | - | 6.6 | | RREB1 | MA0073.1 | chr1:1000462-1000482 | CCTGGGGGGGTGTGGTGTGG | - | 6.6 | | RREB1 | MA0073.1 | chr1:1000252-1000272 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000312-1000332 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000342-1000362 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000372-1000392 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000432-1000452 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000492-1000512 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000522-1000542 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000609-1000629 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | RREB1 | MA0073.1 | chr1:1000669-1000689 | CCTGGGGGGGTGTGGTGGGG | - | 7.16 | | TCF3 | MA0522.2 | chr1:1000949-1000959 | AGCAGGTGTT | - | 6.02 | | TFEB | MA0692.1 | chr1:1001171-1001181 | GTCACGTGAT | - | 6.02 | | USF2 | MA0526.2 | chr1:1001167-1001183 | GCAAGTCACGTGATCA | + | 6.05 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24817 | chr1:999005-1000308 | Colon_Crypt_3 | | SE_34539 | chr1:997968-1000257 | HCT-116 | | SE_65935 | chr1:996609-1000366 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1000831 | 1000953 | | chr1 | 1000736 | 1001492 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001061 | chr1 | 996971 | 1001049 |
|
Enhancer Sequence | GCGGGCGGCC TTGGCCAGGC CCCTCACCGC CACCCCCACG GCCGGATGAG AAGTGGGAGA 60
CGGGGAGCGT TTTGACACCC TCGGAGACCC GGTGTAGCAG GAAGAGCCCA TTGATGGGGA 120
AGGTGGGGGC GGTTGTGCAC CTCAAGCAGG TAAAAGCCCC TCCACAGGCA CCAGGGCCGT 180
GGGCACAGCC TCACCCAGGA AAGCAGCTGG GGGTCCACTG GGCTCAGGGA AGACCCCCTG 240
CCAGGGAGAC CCCAGGCGCC TGAATGGCCA CGGGAAGGAA AACCTACCAG CCCCTCCGTG 300
TGTCCTCCTG GCACATGGCG ACCTCCATGA CCCGACGAGG GTGCGGGGCC CGGGGCAGGG 360
TGGCCAGGTG CGGGGGTGCG GGGCCCGGGG CAGCTGCCCT CGGTGGGAGG GGTGTGGTGT 420
GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT 480
GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG 540
GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT 600
GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT 660
GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG 720
GGTCTGCGGG GCCCTGGGGG GGGTGGGGTC TGCGGGGCCC TGGGGGTGTT GTGGTGGGGT 780
CTGCGGGGCC CTGGGGGGGT GTGGTGGGGT CTGCGGTGCC CTCGGGGGGT GTGGTGGGGT 840
CTGCGGGGCC CTGGGGGGGT GTGGTGGGGT CTGGGGGGCC CTAAGCTTAG ATGCAGGTCT 900
CTCCCTGGCA GCCCCTCAAG GCCACGAGGA TCAGTGCTCG GAGCCTGGAG GGCTGTGTGC 960
AGGAGTAGCA GGGCCACTGA TGCCAGCGGG AAGGCCAGGC AGGGCTTCTG GGTGGAGTTC 1020
AAGGTGCATC CTGACCGCTG TCACCTTCAG ACTCTGTCCC CTGGGGCTGG GGCAAGTGCC 1080
CGATGGGAGC GCAGGGTCTG GGACTGTAGG GTCCAGCCCT ACGGAGCTTA GCAGGTGTTC 1140
TCCCCGTGTG TGGAGATGAG AGATTGTAAT AAATAAAGAC ACAAGACAAA GAGATAAAGA 1200
GAAAACAGCT GGGCCCCGGG GACCACTACC ACAAAGACAC GGAGACCGGT AGTGGCCCTG 1260
AACGGCTGGG CTCGCTGATA TTTATTGCAT ACAAGACAAG GGGGCAGGAT AAGGAGGGTC 1320
AGTCTTCTAA GTGATTGACA AGGTGAAGCA AGTCACGTGA TCACAGGACA GCGGGCCCTT 1380
CCCTCTTAGG TAGCTGAAGC AGAGAGAGAA GGCGGCAGGC ATCAGCGTTT TCTTCTATGA 1440
ACTTATAAGA TCAAAGACTT TAAGACTTTC ACTATTTCTT CTACCGCTAT CTACTACGAA 1500
CTTCAAAGAG GAACCAGGAG TACGGAAGGA GCATGAAAGT GGACAAGGAA CGTGACCATT 1560
GAAGCACCAC AGGGAGGGGT TCAGGCCTCC GGATGACTGC AGGCAGGCCT GGGTAACATC 1620
CAGCCTCCCA CAAGAAGCTG GTGGAGCAGA GCGTTCCCTG ACTCCTCCAA GGAAAGGAGA 1680
CTCCCTTTCC CGGTCTGCTC AGTAACGGGT GCCTTCCCAG ACACTGGCGT TACCGCTTGA 1740
CCAAGGGGCC CTCAAGCGGC CCTTATGCGG GCATGACAGA AGGCTCCCCT CTTGCCTTCT 1800
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