Tag | Content |
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EnhancerAtlas ID | HS019-00007 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr1:1000020-1001720 |
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 |
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| 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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001061 | chr1 | 996971 | 1001049 |
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Enhancer Sequence | AAGCAGCTGG GGGTCCACTG GGCTCAGGGA AGACCCCCTG CCAGGGAGAC CCCAGGCGCC 60 TGAATGGCCA CGGGAAGGAA AACCTACCAG CCCCTCCGTG TGTCCTCCTG GCACATGGCG 120 ACCTCCATGA CCCGACGAGG GTGCGGGGCC CGGGGCAGGG TGGCCAGGTG CGGGGGTGCG 180 GGGCCCGGGG CAGCTGCCCT CGGTGGGAGG GGTGTGGTGT GGTCTGCGGG GCCCTGGGGG 240 GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT GGTCTGCGGG GCCCTGGGGG 300 GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG 360 GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT GGTCTGCGGG GCCCTGGGGG 420 GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGT GGTCTGCGGG GCCCTGGGGG 480 GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG GGTGTGGTGG GGTCTGCGGG GCCCTGGGGG 540 GGGTGGGGTC TGCGGGGCCC TGGGGGTGTT GTGGTGGGGT CTGCGGGGCC CTGGGGGGGT 600 GTGGTGGGGT CTGCGGTGCC CTCGGGGGGT GTGGTGGGGT CTGCGGGGCC CTGGGGGGGT 660 GTGGTGGGGT CTGGGGGGCC CTAAGCTTAG ATGCAGGTCT CTCCCTGGCA GCCCCTCAAG 720 GCCACGAGGA TCAGTGCTCG GAGCCTGGAG GGCTGTGTGC AGGAGTAGCA GGGCCACTGA 780 TGCCAGCGGG AAGGCCAGGC AGGGCTTCTG GGTGGAGTTC AAGGTGCATC CTGACCGCTG 840 TCACCTTCAG ACTCTGTCCC CTGGGGCTGG GGCAAGTGCC CGATGGGAGC GCAGGGTCTG 900 GGACTGTAGG GTCCAGCCCT ACGGAGCTTA GCAGGTGTTC TCCCCGTGTG TGGAGATGAG 960 AGATTGTAAT AAATAAAGAC ACAAGACAAA GAGATAAAGA GAAAACAGCT GGGCCCCGGG 1020 GACCACTACC ACAAAGACAC GGAGACCGGT AGTGGCCCTG AACGGCTGGG CTCGCTGATA 1080 TTTATTGCAT ACAAGACAAG GGGGCAGGAT AAGGAGGGTC AGTCTTCTAA GTGATTGACA 1140 AGGTGAAGCA AGTCACGTGA TCACAGGACA GCGGGCCCTT CCCTCTTAGG TAGCTGAAGC 1200 AGAGAGAGAA GGCGGCAGGC ATCAGCGTTT TCTTCTATGA ACTTATAAGA TCAAAGACTT 1260 TAAGACTTTC ACTATTTCTT CTACCGCTAT CTACTACGAA CTTCAAAGAG GAACCAGGAG 1320 TACGGAAGGA GCATGAAAGT GGACAAGGAA CGTGACCATT GAAGCACCAC AGGGAGGGGT 1380 TCAGGCCTCC GGATGACTGC AGGCAGGCCT GGGTAACATC CAGCCTCCCA CAAGAAGCTG 1440 GTGGAGCAGA GCGTTCCCTG ACTCCTCCAA GGAAAGGAGA CTCCCTTTCC CGGTCTGCTC 1500 AGTAACGGGT GCCTTCCCAG ACACTGGCGT TACCGCTTGA CCAAGGGGCC CTCAAGCGGC 1560 CCTTATGCGG GCATGACAGA AGGCTCCCCT CTTGCCTTCT ATTCACTTCT CACAATGTCC 1620 CTTCAGCACC TGACCCTATA CCTGCCGGTT ATTCCTAGGT TATATTATTA ATGCAACAGA 1680 GTAATATTAA AAGCTAATGA 1700
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