Tag | Content |
---|
EnhancerAtlas ID | HS133-22851 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:124597150-124598970 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:124597648-124597666 | AAAAGGAAGGAAGCAATG | + | 6.19 | EWSR1-FLI1 | MA0149.1 | chr3:124597652-124597670 | GGAAGGAAGCAATGAATA | + | 6.31 | MEF2C | MA0497.1 | chr3:124598469-124598484 | TTCTATTTTTAAAAC | - | 6.49 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00134 | chr3:124593431-124599388 | Adipose_Nuclei | SE_01601 | chr3:124596257-124598531 | Aorta | SE_47296 | chr3:124594568-124605888 | Panc1 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I124875 | chr3 | 124594325 | 124599621 |
|
Enhancer Sequence | CCTAAAAGCC CTTACTTAAT TGGACACAAT ACCAAAGAAA CTCAAAGGAT GTGATAGTCA 60 CCTGGTATGA AAACATCATG AACAACTGTA AAACAATTTG TCATATAGCA TTACTAACTG 120 TTTCTGTTAT TATTAAATAT TCACATGGAA AAGTAAAGTC GTTTGTACTC AAAATGATTG 180 CCCTAAAATT CAGTTGCTGT TGGGACACAT TCAAATTCAA GAAACTCTGC ACTTAACACA 240 CCCTAAACGC TGAGCACTGG ACTGGGGGGA TGCTAGAAAT GCACAGGTGA ATGACCTACC 300 AGCCCTTGAT GTCCAGGAAC TCACAGTGTG CCGGGTACCA GGTACCAGAC AGGTACTCCA 360 GGATCCAAAA CCACAGGCTG TGTGCTGGTA TGTGTAATGT CAGACTCACT CCCTTTGGCA 420 TCTCTCCTCT CTCCACCTAT TAATATTTCA GAGTTTGGAC TTTGCTGGAT GAGTCATTTG 480 GCACCAATAA GCATTTTGAA AAGGAAGGAA GCAATGAATA AAAAACTAAA CACACGGAGT 540 TCACAAATGT CAGTGTTAGG TCTAGGTCAT GGAAACAGGA ACTAGCAGCC CAGATGATAG 600 CCACATCTCA TCTTCTTTGC TGTTTGCATA GTGACTATTC CCAGCTCGGT GGCAACTCCA 660 TGTATCTCTT TTGCCTCACG TCTCTGAAGC CCAGTGTTTA CTGCAAACTG TAATCTAAAA 720 ATATGTTCTT CCAAAATTCA CTGACTCACC CCTGTGTTTC ATCAATCATT CAAGGAGCCA 780 CCGCATCCGG TTGATCACTC CTTTCAAGAT GCAAGAAATG TTTATCCTAA GCCAACCCTT 840 CCTGTCTGCA ACCTCTAGCC CCAACAACCC AAGCCAGGCC CTCTGGTCTA AATTCCTGCC 900 ATAGCCTCCT GGCTGGCCTC CTTCCATTCA GCCTCTCTCC ACTTCTGTAC ACCCCATGGG 960 TCCAAGGTCA GACAACTACT ACTAAAACAT ACATCTGCAG TTGGAATTTC CTGATCCAAA 1020 ATATTCAGTA GGATAACAGA AGTGAATACA GAAGCTGAAA TGGCCTTTCT GCCTTGAAGA 1080 TGGCAATGCC CTGGAATGCT TCTCCCCACA CCCTGAACCA GGCCCTCACA TTTGTCACAC 1140 AATGGACAAA AGAGTCCCAG TATAGACTCC AGCAACTAAA TAGCCATATG TCTAAATGTT 1200 ACCATGAAAT GCAAATATGC CCTAGGAAGG TTCTATCCCA GCAGTTCTCA TTCAAGACTG 1260 CCTTTATGAA CATCAGACAT CTGCACAACA CTCAACAATA CCAGCCTTAC AGATCTGACT 1320 TCTATTTTTA AAACACCAAT TCATATAATG GAGTGCTAGA CAGCTATAAA GAAAGAATGA 1380 GCATGCTCTC TGTATTGACA GGAAGCTTAC CCCAATACAT CGCTAAGTTA AAAATAAAAA 1440 GCAAGATACA TACTGTGTTT TGTGCTGCCT CTGAATAAAA ATGAAAGAGG GATATTCGTA 1500 ACATATCCAT AGAAACCCTC AGGATACATA AGAAAGCTTA TTAGCTTTAT AATAGGAACT 1560 ATATAGGCAC AATTTATTTA GAAAAGGGGG TCACAGAAAT ATCCCACACT GATGGGCAAC 1620 AAGAAAGAGA GGCTTCTCGC TTGATATGAG TTATACTTTT AAAAATTATG GGACTATATT 1680 ACCTATCAAA AGGTATTTTT TTAAAGAGGC AATTGATTAC CTCTATGTTC TTCTTCCAAA 1740 ATCACCTAAC TCTGTCTAAT CACGGGAAAA AATCAGAAAA TCCCAAGAGG GGGATGATCT 1800 ACAAAATATC TGACCAGTGC 1820
|