| Tag | Content |
|---|
EnhancerAtlas ID | HS133-14086 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr18:20694430-20697110 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr18:20695682-20695700 | TCCTCATTCCCTCCTTCC | - | 6.3 | | SPI1 | MA0080.4 | chr18:20695985-20695999 | TACTTCTTCTTTTT | - | 6.19 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_47381 | chr18:20693160-20697090 | Panc1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I023113 | chr18 | 20693609 | 20696950 |
|
Enhancer Sequence | CAGCAAGAAA TGTGTAATTA GAAACACTTC CCGAGGAAAT TAGGTGACAA GTGAAGGCTT 60
GAGGATTTCC GAGGGAGCCT GGAGCTGCAG ATATTCATTA TGGGTACTTA AGAGGCACAG 120
CTGCCTCTGC TGAAAACCAT GTCAAATGCC GTCCGCTGGA TGCCAGCGTG GAGGCCAGCC 180
CAGAGCCAGA GATGGTGGCT ATGGCAACAC GCTACTCCAT TTTTAAACTT TTCATTACCT 240
AAAAGGAAAT TGCTTAGGCT GTTTTTCTTT TTTTCCTTTT TCTCCCTACC AATTTCAGAG 300
TTTGTACCAG CAGTGAATAG CCTCCAGGTC TAACATTTCC TGGGTAATGA GTGACTAGCT 360
GGGTGAAGTG CTTTTGGCCT TACCTCCAGC CTTGGCAACT CCAGCCAGTT ATTAATTGCT 420
GCACCGGGAA ACACTTTCCA ATCAAGCTAT TATTTAATCA AAATAAAAGA AAACGAACTA 480
TTATTGCTGT CAACAGCAAT GAGCAACTCT CCGCAGGAGT CTAAATGGGA ACTGTGGAGG 540
TTTTCACTGG AAGAAGTGTT CCTCTGGGGG TCAGATAAGC AGGGCAACGT GAAGTTGCGT 600
GGAGTACCCT TGGGAACTGG TTCTTGTGGG AGGAGAGAAT GTTGAACCAG CAGGAAGACG 660
CAGAGAGATT ACACACACCC TGTCCTAGAT CTCAGTCATT CATGGTCAGT TAACCTGTAA 720
CCTTGCTGTT AAGCCAGTGC CCCAAATGCT TCTGTGGGAG TGTCTGCAGG GGAAAAGACA 780
GTCCATAGAA GCATTTGGGC TGCTTCTATA AGCAATAAAT AGTAAAACCT GTAACCACCA 840
TAATAACCAC ACTTCCTGAG TACCCCCAAT GTGCCAGGCA GGCACTGTGC CCCCAGGTTT 900
ATACTCAGAT CTCAAGAGTT CCCCACATTG CCACTGTGGG GAGAGTATAG TCACGATCCC 960
TCTTTCACAG GGACACTGAG TCCGAGAGAG ATGAACTTGG CCAAGACCCA CCACACCCTG 1020
GTGTGAATAG CAGAGCCGGG GCTTGACTTC TAGTCTCTGC ATCGAGCAGT TGCTTTTTTT 1080
TTTTCTTTAA GTGACAATAT AAACATAACA TAAAAGTGAC CATCTTAACC ATTTTTAAGT 1140
GGATAGTTCT GTGGCAGTAA GTACATTGAC ATTGTATGCA ACTATCACCA CCAACCATCT 1200
CTAGAACTTT TTCATATCCC CAGCTGAAAC TCTGTACCCA TTAAACACTA ACTCCTCATT 1260
CCCTCCTTCC CCAAGCCCCT GGCAACCACT ATTCTGTCTC TAACAGCGTG ATGATTCCAT 1320
GGACCTCACA TGAGTGAATC ATACACTATT TGTCCTTTGG TGACTGGCTT GTTTCACTGA 1380
GCGTAACGTC CTCAGGGTTC ATCCACGTTG TAGTATGAGT CAGAATTGCC TTCCTACTTA 1440
AGGCTGAATT ACATTCCATC GTTTGTATAC ACCACATTTT GTTTATCCAT TCATCTATGG 1500
ATGGACATTT GGGTTGTGCC CATGTTTTGG CTGTTGTGAA TCATGCTGCT ATGTTTACTT 1560
CTTCTTTTTT TTTTTTTTTT TTGAGATGGA GTTTTGCCCT TGTTATCCAG GCTGGAGTGC 1620
AGTGGCATGA TCTTGGCTCA TTGCAAGCTC TGCCTTCTGG GCTCCAGCGA TTCTCCTGAC 1680
TCAGCCTCCC GAGTAGCTGG GATTACAGAT GCCCACCATC ACACCCAGCT AATTGTTTGT 1740
ATTTTTAGTA AAGGCGGGAT TTCATCATGT TGGCCAGGCT GATCTTGAAC TCCTGACTTC 1800
AGGTAATCCA CCTGCCTCGG CCTCCCAAAG TGCTGGGATT ACGGGTGTGA GCCACCGTGC 1860
CCGGCCGCTA CGTTTAACTC TTAACCTCTA AGATTCATTG CCCCTGGGAG TAGTTGCTCT 1920
TCAAGGATAA CACATGGCTC AGGGACTGCC TGTCACACCC CAACCTGAGA ATCAGCAGAG 1980
ACTACCACGG GGCCCATCAG GCCACTAGGC AGGTGCCACT CCCCTGGCAG GGAGAGAGGT 2040
GCCGGTGGCC ACCGACCTCA TAGGGTTCCA CAGCTCCACA CTGGCATGTT GCGGGAGGAA 2100
TTTCAGTGTT CAATCCCAGG CTGTTTCTCT GAGTCTTAGG TTCTGGGATA AACAAGCTCC 2160
TTCAAGTCCA AACTGCTCAG ATTAGACTTT ACTGATAGAT TCCACACCTG GAATCCTGCT 2220
CCGGGACTGC AGTCTCATCC TCCAGCTCCT GCAGGCTTCT TCTAAGCTGG TGGGTCTCAG 2280
CAGGGATGGG GGTGAGTGGT ACTCCACACC CAGGGGACAC CACCCACAGG AAGCTTTGTG 2340
GACATGTGAA GGGCATATGT GGTTGTCATA ATGGTTGGGG GACACTGTTA ATATTTATGT 2400
GAGGCCAGGG ACTCAGGTGA CCTGCAGTGT GTGAGGCAGT CACCCACAAC AAAGAATTGT 2460
CCTGCATCCT GAACCAATTT CAAACAACCC ATTAACATTT GTCTCCTAAG CTGTGTGACC 2520
TAAGTGCCAC CTGCCTCCCC GGTTCCTCTC CCTCCCCTCT CATGCTTAAA GATAAGCCAT 2580
TTTTGGGCCG GGCACGGTGG CTCACGCCGG TAATCTCAAC ACTTTGGGTG GCCGAGGCAG 2640
GCGGATCACA AGGTCAGGAG TTTGAGACCA GCCTGATCAA 2680
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