Tag | Content |
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EnhancerAtlas ID | HS134-03539 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:164651900-164653000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:164652259-164652277 | GGATGGAGGGAAAGAAAG | + | 6.16 | EWSR1-FLI1 | MA0149.1 | chr1:164652088-164652106 | CATACCTCCCTTCCTTGC | - | 6.25 | IRF1 | MA0050.2 | chr1:164652624-164652645 | ATATTCTTTCACTTTTATTAT | + | 6.69 | ZNF263 | MA0528.1 | chr1:164652256-164652277 | AGAGGATGGAGGGAAAGAAAG | + | 6.23 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27676 | chr1:164651094-164655910 | Fetal_Intestine | SE_28616 | chr1:164650944-164655444 | Fetal_Intestine_Large | SE_68010 | chr1:164599817-164697547 | TC32 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I164682 | chr1 | 164651245 | 164654042 |
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Enhancer Sequence | TTCTTCTACT GTTAAATAGC AACCTCATTC CTCAGGCTGC TGATGGAATT GGTAACTGAG 60 TAATCAGGCC ACTGTGCTCG GGGACATAAA ACCTGTGGCT GCTGCCATTG CAGAGTCCCG 120 TCATGGATCA GAGTTCGTCC CTGGGAAACA ACTTGTGCCG ACGGAAGGAG TTCTTCCTTT 180 GCTCCCCTCA TACCTCCCTT CCTTGCAGAT GGGATCCTTG CAAGGGCAGA GCAGCTCTTA 240 GAGTTGTCAG GCCCTTTTCT TTCATTCTGC TTATTTTCCC ATAGGCGAGT ACTGCTCAGA 300 ACCCAGGCTG TGAGTTTTTT GATGTGGAAA GCTATTTACT AAGCATGTCT TGACGCAGAG 360 GATGGAGGGA AAGAAAGCCT CCAAGAGAGT GGTGATTCTA CAACCATCAT CAAATTTTGG 420 TTGAAAACTC AAAGCTGCTG ATATGTATTA GTAAGCAGAT AACAGTAACA TCCTGTATTT 480 GCATGGCCCT GTATCAGTCA ATAGCATTCA GATTTGTGTG GTGGTGTATA GCTTTCCTTA 540 TTTCATATCA GGTGTTTTCA TTTGATCCCA AGTGGTATGT CCTGAGACAG AAGAAATAGC 600 CCCATTTTAC AGAAGAAGAA ACCCAAAATT GCAAGGAATT TGCCTAAGGT CATTAGAAAG 660 TGTCTAAAAT AAGACTTTGA CCCGGACTCT CTGATTTCAA GCCCAGCGAT TCTTCTAACA 720 GGCCATATTC TTTCACTTTT ATTATCTTGA CTTACGCAAC AAAGGAGATA AGCCAGGTAC 780 ATGTCATTAA TCTTCCTATG TATGACAACT GAGGCTCCAG GAGGTTAAGT GCCTTGCCTA 840 AGATTACTTG GGTGGTGGTA GAACTGGTTT TCAAAACCAG ATCATCTGAA TGGAATCTAA 900 GTCTTTCTTC TGTATCACCT TGTTAATGTG TCAGGAACTA CCACCCCACC TTCCAAAACA 960 CATACACACT CTCACTTTTA ATGCGGACCC ATCTTAGAAT AAACTAGTTA AGGACTGACT 1020 GCTGAACATG GTCCAGAAAC TTACTGTCAA ATTTTGCTTT TGAGATGTGC TTGTGTTGTG 1080 TGAAGTCTTT TTTTTTTTTT 1100
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