Tag | Content |
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EnhancerAtlas ID | HS098-13192 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:53370510-53371920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:53370981-53370993 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53370985-53370997 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53370989-53371001 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53370993-53371005 | AAACAAACAAAC | - | 6.32 | Foxo1 | MA0480.1 | chr12:53370687-53370698 | TGCTGTTTACA | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28539 | chr12:53368573-53370700 | Fetal_Intestine_Large | SE_43402 | chr12:53368192-53371633 | MCF-7 | SE_47355 | chr12:53367961-53371751 | Panc1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052974 | chr12 | 53368170 | 53371635 |
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Enhancer Sequence | ACCAGATGAG GGAGCCATAA GGGATGCAGA CAGAGACTCA AAGACAGAGA CAAGGGCTGA 60 GGGAGGGGGG ATGGAAAGAA CTGGGGAGCC AAAGACTGCA GCGGGGAAAG AATGCAGTGT 120 CCATCCTAAA AGAAGGAAAA TGGAAGTTTC CCAGGGAGGA GGGTGCCTGA TCTTATCTGC 180 TGTTTACATT CCAGAGAGCC CCTGCTTCTG CTTCTCATCT TAATTAGAGA ATACTTGAGA 240 AGCCCTGCCG CCGTGCAGAG AGAAAGGAAT GCAGGCCCCC ACTAAACCCC AGCCTGCCCC 300 CCTCACCCCT GACCTCCTGC TGGCTATGTG GTGGGACTGA TGGGAGTCTG GGTTCTGGAT 360 CCATTTTCTG TTTTCTGTTT TTTTGTCTAC AGTGGGCTGA TCCATTAAGC TGGATTCCTT 420 GAGAGAGTAT GTGAGAGGGT CTGGGAACTG TCAGGGCTCC ACTCCTGCAG GAAACAAACA 480 AACAAACAAA CAAACAAAAT TAAAAAGTAT TAGAAAGAGC CACTGAGAGG AACAGCTGAG 540 ATTCTCTCAG TCAGTCTGCC ATTCACCCCC TCAAACATCG CCCTCACTCC ACCACCATAA 600 TGTCCAGGCA GGGTGCTGAC ACTTCACCGT TCACCTCCCA CCCTGCCCCG GGCTGTCCTC 660 CAAATGTGTG TCAGACACAG TGCTGGGGGA CTTATACTTC TGTCATAGTC TCTGTCTTCA 720 GTAGCATATG GTAAGAGCCA GGATCCGCTA TTAAACATGC TGTGAGTGGG TAGAGACAAA 780 GTCTTGTCTT GTAGGGTGAG CAGGCAGTGA GGTCAGAAAG GGCATCACAG GTAGAGGAAA 840 AAGCATGGGC AGAGGTCTGG AACCCAGTCC CTCTTCATAC CACCCGCTGA CCCTTTCCCC 900 TCCCCCCCAC ATGAGATTTC TCCCCCTCTC TTCTCTCTTC TCTCCCTCAA CAATTCCAGG 960 GTTGCCCACC TGAAAACAAG CTCCCTGGAC CACCTTCCCT TGCAGCTCTC TGTTCCTTCT 1020 CTCTTTTTTT TTTTTTTTTT TTTTTGAGAC GGAATCTCAC TCTGTCACCC AGGCAGGAGT 1080 GCAATGGTGT GATCTCAGCT CACTGCAGCC TCTGCCTCCC AGGTTCAAGT GATTCTCCTA 1140 CCTCAGCCTC ACGAGTAGCT GGGATTACAG GTGCCCACCA CCACACCCAG CTAATTTTTG 1200 TATTTTTACT AGAGATGGTG TTTCACCACA TTGGCCAGGC TGGTCTCGAA CTCCTGACCT 1260 CAGGTGATCC ACCCGCCTCA GCCTTCCAAA GTGCTGGGAT TACAGGCGTG AGCCACTGCG 1320 CCTGGCCAGC TCTCTGTTCC TTCTCATAGC TAAGCATCTT ACATCATTCT CTCTCGTTTT 1380 GTTGTTGTTT TGTTGTTGTT GTTGTTGTTG 1410
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