| Tag | Content |
|---|
EnhancerAtlas ID | HS133-06814 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:1949990-1951820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr12:1950972-1950986 | CTGCCACGTCACCA | + | 7.42 | | KLF14 | MA0740.1 | chr12:1951379-1951393 | AAGGGGGCGGGGCC | - | 6.15 | | KLF16 | MA0741.1 | chr12:1951381-1951392 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr12:1951382-1951392 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr12:1951774-1951794 | CACCCACCCACCCTCCCACC | + | 6.18 | | SP4 | MA0685.1 | chr12:1951378-1951395 | GAAGGGGGCGGGGCCCA | - | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33402 | chr12:1927823-1955818 | H2171 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I001841 | chr12 | 1950881 | 1951041 | | GH12I001842 | chr12 | 1951367 | 1952061 |
|
Enhancer Sequence | GAAACAGAGA CAACCCAGTC ATGGGGAAGA GCTGTGGTTG GGGCAGGTGG AGCGCTACCA 60
CTTTCTTGGA ATAGGAGATG GGAATAAAAG CAGGCGAAGG CATCCTTGGA AGAATTGAGG 120
CGAGGGTGGG GACAGGGGTT GTGTTTGGAG AAGTTGCTGC TGTGATGGTG ACCCCAACAC 180
GGGTCTTGGA CAGACACACA CATGGCCTCT GGCCGCCAGC ACAGTGCAGG GCTGCAGTGG 240
CCCCACGACA CTGGGGTTTC TGCGTGTTTG TCGGCTGCGG CATGCATTTT GCCCACAACA 300
CCTGTGTTGT ATCCAGTGAT CCCTTCCAAC GGCAGGAAGG ACAGGCTGCA TTTCAGCACT 360
GGGTGGTGGG TGATCCTGGA TTGCTCTCTG TGAGTCTGCG TGAGTCAGGG AGGACGCCGA 420
CAGTCAGTCC CAATCAGGAA GCCAGATGCC ACAGCCGAGC CACCATGCGG CCCTGGGCAG 480
CGAGATGACG GACCCTCCAC TGCACAACCG CTCTCCGGGT CTTTCACTTG CTTCTCAGCT 540
GTTGCTCCAC TTCTGGGACT CTGCAGCAAC TCAGGGCAAG TCCTGAGGCT CCTGAAGGCC 600
ACAGGGCTTG CCTCGCATTG CTCTCTCCAC TTCTTCTGGA ACAATCAGGC CACCATAGGT 660
GCACAGTTTA GAGGGCAGTT TCAGCTCCAC ATTGAAACAG AGCTTTCTGG TTCTGACTGG 720
GGCTGGCTAC TTCGGGGCCT CAGGCTTCTT AATTCTCATC AGTCCTTGGC CCCGGACTTG 780
AATTTCAAAG CACTCTTGTC TGCAGGTCAA ATGCAGACTC AACTTCTGAG AAAGGGGCAA 840
ACAGTTTCTG ATGTGCTATC ACATTTTGTT AGAATGTCTT GATGTCAAAT GTTGCCTGAA 900
GCAAACAGGT CATGGGACTC TTGTGTGGCG ATTATGACAA CAGTGTCAAT TGTCCCGGGA 960
CTTAACCACC AGCTTCTCAC ATCTGCCACG TCACCAAGAT TACCCATCAC ACCCGCTGTC 1020
GTCAAATATC TCAAGAAACC TAAAACTGCA GTCTGATTCC AGGAACTTCC AATATGTAAG 1080
GTTGTCCTTG ATTCTAGAAA TTTGCCCCAT GATGACGAAG GGACAATTCC CCACCTTGTG 1140
TCTACAGACA TCTCGAAGGT GGTGATGTGG CAGCCCCGAC AATATTCCCT GGGTCCCACA 1200
GCCCATTTTC TGGGACAGAC CTTCCGTCGC ATTTGTACCC CAGCCAGCAG AGGCTTGTAG 1260
GAAACGCAGA TGTGAGCATG TGGAGACCCT AATGAGGCAG TCTCTGGGGA CATCAGGGAT 1320
TTCAGTGCCT GGCTCACCGT GGCTACCTGG CCCAGCACCT GGTGGGAATG ATCAGGGCGT 1380
GGAGTGCAGA AGGGGGCGGG GCCCAGGGAG AGGTGGGCTG TGGGCATATT TCTGAGGCTC 1440
TGCTGTGTGC GGACAGGTTT CTAGGCACTG ACTGCACAAT GCAGCTCCAC GTGGTCGGGA 1500
CTTAGCCCAC CAGGCCCCGG CAAAGGGCAA CCATGTCAGC CTAGAGAGAC AGGCGAGCTT 1560
CCCCTCACCC TGGAGGCAGC TCGTCCTCTT TTCCCCCTTG AAACGCGGTT GTTTTCCTTC 1620
TTTTGGGGTG GAAGGGAGTG TGCAGAGGTG GCCATGTGTC TAAGCGTGTG TGTGCGCTGA 1680
GCGAGTGAGT GGGCTGTGGA GAGGAAGTGG GCCCCGCCTC CCTCCTCACC AGGCCCCCTT 1740
TTTGGGCTCC AGCTTCCCTC TTTTCTCCTC GTGGCTCAGC TTCTCACCCA CCCACCCTCC 1800
CACCTCATCA CCACATAAAG CTCCCCCAGC 1830
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