Tag | Content |
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EnhancerAtlas ID | HS002-01209 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:229160130-229161310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr1:229160551-229160566 | CTGATGACTCAGCAG | - | 6.16 | MAFF | MA0495.3 | chr1:229160551-229160566 | CTGATGACTCAGCAG | + | 6.1 | MAFK | MA0496.2 | chr1:229160549-229160568 | CTCTGATGACTCAGCAGCA | - | 6.18 | NFE2L1 | MA0089.2 | chr1:229160552-229160567 | TGATGACTCAGCAGC | + | 6.42 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_49843 | chr1:229153562-229162649 | RPMI-8402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I229024 | chr1 | 229160142 | 229161146 |
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Enhancer Sequence | CAAGCATGAT AAGGTCTCGT CACTGTGTCT CCAGGATCTG ATCACTGCAG ACCCTGGGCA 60 GTGATTAGGG AGCATGGGCT CTGGAGGACC AGCGCCTCTG ACTCTCTATG GCCCCGGGCA 120 AGTCTCCAGG TCTCCATTGC CTCACCTCTA AAGTGAACGT AGAGTCTAGA ACGTAAGCCA 180 GTGCGTGCTG ACGGTCCCCA CACCGCACTG CCAGGGGCCT CGGGCTCTGC TCTAGCAGCT 240 TGGCCTGGAC CACGGAGCTC TTTGACCAGG ACCTGCTCCA CCTGAGGCTG ATGCCCTCAT 300 GGTGCTGCCT GGCCCAGCCA CGCCCATGAT CCTTTTCCAG GGTCCCGGAG AAGGAGAAGA 360 ACTTCCTTTC TGGTCCTTCC CATTCTGCTC CTGGGTTCAA CCAAGCAGCT TCTAGGCAGC 420 TCTGATGACT CAGCAGCAGT GACTCACAGG TTCCCAGGAC AGCAGATGAA TCCTCTGCTT 480 CTCTGGCTCC CTCTCCGTCC CCTGGCTCTT CCTGGCAATG TGCTTTCACT CAGCCTTGGG 540 CCCACTTTCC CATCCCTCTG GGGACATACC CCCTCGCTTG TCCTGAGACC CACAGTTGAG 600 ACCCACACCT GGGCTCCAGC CTCTCTACTG TTCTTTTTAC TTCCCAAGCT GGCCCATGGT 660 CCCTTCAGGC TCAGCTCTCC AGGGATCTGC TACCCCGTTC CTGCCTCCGG GACCCACTCC 720 ACCCTCCTGG CACTGGCTGG GTCCTGGTGG AGGAGCTACC ACAGGCAGCA GAGAAGCAGA 780 ATTCTGCTGA GAGCTGTGAC CCGAGGACAC TGGGCCCCAC CAAGCCCACG GTGCAGACCC 840 TGGACTGCTA GAGAGGATGG CAGCACCATC CCCTCCAGGA AGAGCCACCA GGCCTGGAGG 900 AAAACCTGCG CCTCTGAGAG CCTCAAAGGA GCTGTGCCAG TCAGAAGGTG CCGCTCAATG 960 GTCCTGGTCC TCTGGGGGTG ACAGGGTCAC ACTGCGAGCC GGACTTTACA CAGCACATCA 1020 GTGTGAAGGA TGCCAGCATC CTTGTCTGTC ATCTTCCTAA TTATGAGCCT GCTCAACCCC 1080 TCCCCAGCCA CCTAGCTCAT GCAGGGCCTT CGCTTCTTTG GGCCTTTCCC TCCTTCATGC 1140 CATGAGAAGT AAAGGCCAAG AAGGGTCGCA GGACATAGGC 1180
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