Tag | Content |
---|
EnhancerAtlas ID | HS133-06754 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:133804070-133805510 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:133804882-133804893 | GGGCGGGAAAG | + | 6.32 | INSM1 | MA0155.1 | chr11:133804875-133804887 | TGCCAGGGGGCG | + | 6.74 | ZNF263 | MA0528.1 | chr11:133805357-133805378 | CTCTCCAGCCATCCCTCCTTC | - | 6.14 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41022 | chr11:133803845-133805747 | Left_Ventricle |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I133934 | chr11 | 133804491 | 133805405 |
|
Enhancer Sequence | ACAGGGAAAA CCAAAACATG TCTCCAGAAA GACAGATGGC CTATGGCTTC GAGGAGGGGC 60 CTTCATCCTG GCCAGCTCGT CTTCCAAAGG CCACCTCCTG TTGGCTCCTC CTGCCCCACC 120 ATGGCCAACT CCGTGCCAGG TGGCACAGCC TGCGTCCAGC ACAGAGGGAC GGGGCGCACC 180 TTTGTGGTGG ACGGGTCTCT CCTTCCTGCA GCTCTTCCCC ACCCCAGCAC AGCTTGGGCA 240 CATCCTAAGT CATGTATGAA TAACTTCTCA ACTCGCTTTT TCCCGCTGCA GGTCTGGGGA 300 GTGAGATCTG TTGTCCTGGA CCTCACGGCT CTCTAAAGCT TGGGCCTGGG AATACAGCAC 360 ATCAAAAGTC CTTTAAGTGG CTGACGGCAG ACGCAGAGAG GCGATGCACT CCATAGAGAG 420 GAAAGAGTGA GACTGCGAGG TTAGGGGTCC GATGGCGCTC AGCAGGCGCA GCGTGCTCCA 480 CCACCGCGAC CAGTGGTGGA ATGTCCACAT CCAGCTCTGG GCAGCAGTCG GACCAGCTCC 540 ACCTCCAGGG CCACCAGCCA TCCTCCACTT GTCCTCAGCT CGTACACTGA CCCCGGTCTT 600 GTCTCCAGAC TGTTCCACTT CTCACCCCTG CCACTCCCTG TCGCTGGGTG TGAGCAATCC 660 GCCCACACCA GCCGGGAAAT GAGGGAGAGT CTGTTATCTA CAGCAACAAT GCCAGCCTTT 720 GTTGCCTGAG TGACAGGGCC ATCCACAAAT CAAAAGGAAG ATATTACTCC TCATTACTCA 780 TCCTTCTCTG TCTCAGGGCT CAGCTTGCCA GGGGGCGGGA AAGCAACTGG CGGCTCAGTA 840 TTAAAGATCA GCAAGCTGAA TGGTGGTGCT TGCACAAAAG CCCTCGAACG TCTGGGTGAG 900 GAGCAGCTCA TTCATCTGGA TCTCCAGCCA CCCAAGGGGA GAGGCCGCGG ACGCCAGAGG 960 GAGCAGGCGC AGGAGCTGGA GCACATCGCC CCCGACACAG ACGCGGTGTG GAAAGGCAGG 1020 GAGTAAGGCT GGGAGAAACC TAACCCTGCA TGGGCCTGGG CTATGCTCCA TAAGACACCT 1080 GAGAAAAGAG CACCAGAGAG CAACTGATTC TGGGCACAGA GGTGCAGGCC AGCCTTCAGC 1140 CCGAGGACCA CCGTTCAGAA GGAACTGCTC AAAGGTGTCT TCCTGAGTGC AGCCTGCACG 1200 GAGCTGATGA GATGTACTGG CTGAACAGCG ACGCCTGGCC AGCGAAGTAG GAGCTGCTCC 1260 ACCCCAACTG TCCAGGGCCT CGGCCTCCTC TCCAGCCATC CCTCCTTCTT CTCTTATTCG 1320 CTCCTCCACC TACATGCCCC CAAATGATGC TTGGTCTTTG CTACCCTCCA GCCTACAGTC 1380 TGGCTAACAC CAAAACCTTC TGGGAGCCCC ACCACCCAGG CTCCCCTGCA CCCCTACTCA 1440
|