Tag | Content |
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EnhancerAtlas ID | HS047-27957 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:172086190-172087380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:172086564-172086582 | GCATGGAAGAAAGGAAGG | + | 6.5 | TP53 | MA0106.3 | chr5:172087022-172087040 | GACTTGTCAGTGCATGTA | - | 6.13 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23380 | chr5:172085235-172087702 | Colon_Crypt_1 | SE_24236 | chr5:172085268-172087575 | Colon_Crypt_2 | SE_27137 | chr5:172085104-172089457 | Esophagus | SE_28885 | chr5:172085115-172089093 | Fetal_Intestine_Large | SE_40610 | chr5:172084985-172090207 | Left_Ventricle | SE_48563 | chr5:172085014-172089981 | Right_Atrium | SE_50624 | chr5:172085114-172089312 | Sigmoid_Colon |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I172657 | chr5 | 172084594 | 172093195 |
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Enhancer Sequence | CCCAGCTGTT GGGGTGTGAA GAACATTTCT TCAGTCCAGG AGCAAGAACA GTGTTGCTCC 60 AGGGGAACTT GGGCCAGTGG GTCTATTGTG CCAAAAATGC TGACCTTCAG GCCCCGCAGG 120 TGCTCTCCTG GGGCTGAAGT TGGGAGCAGC CAGGCTTCTG GGCACCACCC AGGCTGGGGG 180 AGTGGCTGTC CTCAAGGCAA AGAGAAGGAG AAACGGTAGG CCTGGCAACC TCAGCCAGCT 240 TATCACTGGG CAGCTGCCAG GGGCTGCCAG GAGGAGAAGC AGGCGCTGAG GGGCAGGACC 300 ATGTCAGCCG TTGGAAGAGA CATTCAAAAC CTGGACTGTT TTCTTACTCC TGCCACGCTG 360 GGTCACTTTG ACTGGCATGG AAGAAAGGAA GGCCCAGGGT TTCAATCTCA TTTTTCAGAG 420 AGGTGGATCC ACAGGAGTTT TTCTTCCCTG ATCCCAACCC TTCAGCAGCC CCCAGAACCT 480 TCTGGAGGAC TTTAACCTCC CCTGCATGGC CTTTAAGACC CTTTGTGATA CTGCCCCTGA 540 CTCCCACTCC ACCCTCCCCT CTCCCTTCTG GCCTGTACTC CTCACAGTTC CCCAGTGCTC 600 TCAGCTGATT CTCATCTCCA GGCCTTTGCT GGTGCTGTTC CCTCTGCCTG AAACACACTT 660 CCCCATCCTT TGTCATCCTC CCAGCCCTGC TTCCTCAGTC TGCAAAGCAG CTCCCCTGAG 720 AAGCTGTCGC CACTGCCCCA GCCCTCCCTG GCCACCACCC TGTGCAGTCA TGGGGTCTGC 780 TTATGTCCAT CCTTGCAGCT GGTCTCAGCT CGAGGGGGCG GGGACAGTGT GTGACTTGTC 840 AGTGCATGTA CCCGGCAGCC AGCGCGGGCC CTGGCCCAGA GCAGATGCTC TGTAAATGTC 900 AGATGAAGGA GGAAGTGATG TACTCGAGAA GGAATGAGGG CACATTCCCC CCACCTCTCA 960 CTGCAGTGGG GCCCTAGCCC TGGGAGCCGG CGCCTCTGAA GTTGGAGTTT CCTGGGTCCC 1020 TTTATCAAGA AGAGACCACA GTCAGGGGGC CCGGCAGAGG GTCGGAGTCA GCTTGGGAAT 1080 CCCAGCCCTG GCTGAGCATG CTTTGAGGGG GCGTCGGGAT GACCTCACCC CCTGGGAACT 1140 CTCGCATCAG AGCCCACTCA AGCTGAGAGG TCTGCCACTT AGGCCTGGAT 1190
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